Non-Alcoholic Fatty Liver Disease,Robinow Syndrome, Autosomal Recessive 1,Charcot-Marie-Tooth Disease, Dominant Intermediate C,Neuromuscular Disease,Fatty Liver Disease,Infantile Liver Failure Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2d,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Retinal Degeneration,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Hyperinsulinemic Hypoglycemia,Charcot-Marie-Tooth Disease,Fatty Liver Disease, Nonalcoholic 1,Charcot-Marie-Tooth Disease, Axonal, Type 2n,Tooth Disease,Rigid Spine Muscular Dystrophy 1,Charcot-Marie-Tooth Disease, Demyelinating, Type 1b,Charcot-Marie-Tooth Disease And Deafness,Visceral Steatosis, Congenital,Charcot-Marie-Tooth Disease, Recessive Intermediate B,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Combined Oxidative Phosphorylation Deficiency 8,Charcot-Marie-Tooth Disease Intermediate Type,Charcot-Marie-Tooth Disease, Axonal, Type 2u,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Charcot-Marie-Tooth Disease, Dominant Intermediate A,Developmental And Epileptic Encephalopathy 29,Perrault Syndrome,Usher Syndrome, Type Iiib,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Charcot-Marie-Tooth Disease, Dominant Intermediate D,Neuronopathy, Distal Hereditary Motor, Type Va

Robinow Syndrome, Autosomal Recessive 1,Pelizaeus-Merzbacher-Like Disease,Leukodystrophy,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Fibrosarcoma,Developmental And Epileptic Encephalopathy 29,Ectodermal Dysplasia 1, Hypohidrotic, X-Linked,Robinow Syndrome,Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism,Autosomal Recessive Non-Syndromic Intellectual Disability,Hypomyelinating Leukodystrophy,Leukodystrophy, Hypomyelinating, 3