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,Bulbar Polio,Trichohepatoenteric Syndrome 1,Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements And Lactic Acidosis, With Or Without Seizures,Spastic Quadriplegia,Lactic Acidosis,Perrault Syndrome,Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

Sideroblastic Anemia,Myopathy, Lactic Acidosis, And Sideroblastic Anemia,Myopathy,Charcot-Marie-Tooth Disease, Dominant Intermediate C,Mitochondrial Myopathy,Combined Oxidative Phosphorylation Deficiency 12,Charcot-Marie-Tooth Disease, Axonal, Type 2d,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Optic Atrophy 1,Mitochondrial Disorders,Charcot-Marie-Tooth Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2n,Rigid Spine Muscular Dystrophy 1,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2,Charcot-Marie-Tooth Disease, Recessive Intermediate B,Lactic Acidosis,Optic Atrophy 5,Combined Oxidative Phosphorylation Deficiency 20,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Charcot-Marie-Tooth Disease Intermediate Type,Sideroblastic Anemia With B-Cell Immunodeficiency, Periodic Fevers, And Developmental Delay,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Perrault Syndrome,Mitochondrial Dna Depletion Syndrome 4a,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 3,Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes,Pearson Marrow-Pancreas Syndrome,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1,Neuronopathy, Distal Hereditary Motor, Type Va

Robinow Syndrome, Autosomal Recessive 1,Noonan Syndrome 1,Charcot-Marie-Tooth Disease,Neuronopathy, Distal Hereditary Motor, Type Ix,Charcot-Marie-Tooth Disease, Axonal, Type 2u,Developmental And Epileptic Encephalopathy 29