Cardioencephalomyopathy,Mitochondrial Dna Depletion Syndrome,Seizure Disorder,Degenerative Myopia,Myopia,Hypertrophic Cardiomyopathy,Complement Component 2 Deficiency,Mitochondrial Metabolism Disease,Anisometropia,Mitochondrial Neurogastrointestinal Encephalomyopathy,Refractive Error,Spinal Muscular Atrophy,Muscular Atrophy,Mitochondrial Complex Iv Deficiency, Nuclear Type 1,Rare Isolated Myopia,Leigh Syndrome With Cardiomyopathy,Dilated Cardiomyopathy,Myopia 6,Cycloplegia,Mitochondrial Disorders,Charcot-Marie-Tooth Disease,Juvenile Glaucoma,Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due To Copper Metabolism Defect,Mitochondrial Dna Depletion Syndrome 2,Mitochondrial Dna Depletion Syndrome 1,Mitochondrial Dna Depletion Syndrome 4b,Lactic Acidosis,Mitochondrial Complex Iv Deficiency, Nuclear Type 2,Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Dna Depletion Syndrome 3,Spinal Muscular Atrophy, Type I,Cardiomyopathy, Infantile Hypertrophic,Kearns-Sayre Syndrome,Leigh Syndrome,Myoclonic Epilepsy Associated With Ragged-Red Fibers,Neuropathy, Ataxia, And Retinitis Pigmentosa,3-Methylglutaconic Aciduria, Type Iii

Cardioencephalomyopathy,Mitochondrial Complex Iv Deficiency, Nuclear Type 4,Hypertrophic Cardiomyopathy,Alzheimer Disease,Mitochondrial Complex Iv Deficiency, Nuclear Type 1,Mitochondrial Disorders,Gracile Syndrome,Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency,Mitochondrial Dna Depletion Syndrome 9,Leigh Syndrome