Mitochondrial Dna Depletion Syndrome,3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome,Mitochondrial Encephalomyopathy,Muscular Disease,Intestinal Pseudo-Obstruction,Mitochondrial Dna Depletion Syndrome 12a,Retinitis Pigmentosa,Migraine With Or Without Aura 1,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1,Myopathy,Status Epilepticus,Seizure Disorder,Spinocerebellar Atrophy,Epilepsy,Optic Nerve Disease,Mitochondrial Dna Depletion Syndrome 12b,Muscle Tissue Disease,Cortical Blindness,Mitochondrial Myopathy,Mitochondrial Metabolism Disease,Parkinsonism,Axonal Neuropathy,Mitochondrial Neurogastrointestinal Encephalomyopathy,Male Infertility,Plagiocephaly,Febrile Infection-Related Epilepsy Syndrome,Spinocerebellar Ataxia 20,Chronic Progressive External Ophthalmoplegia,Mitochondrial Dna Depletion Syndrome 7,Motor Peripheral Neuropathy,Central Nervous System Origin Vertigo,Myotonic Cataract,Diabetic Polyneuropathy,Ocular Motility Disease,Hypertrophic Olivary Degeneration,Acute Necrotizing Encephalitis,Infertility,Autosomal Dominant Progressive External Ophthalmoplegia,Mitochondrial Complex Iii Deficiency, Nuclear Type 2,Mitochondrial Dna Deletion Syndromes,Cerebellar Disease,Mitochondrial Dna Maintenance Defects,Mitochondrial Disorders,Obesity Due To Melanocortin 4 Receptor Deficiency,Polg-Related Disorders,Dystonia,Fanconi Anemia, Complementation Group I,Testicular Germ Cell Cancer,Neuropathy,Germ Cell Cancer,Acute Liver Failure,Charcot-Marie-Tooth Disease,Cranial Nerve Disease,Visual Cortex Disease,Parkinson Disease, Late-Onset,Early Myoclonic Encephalopathy,Peripheral Nervous System Disease,Polyneuropathy,Premature Menopause,Ataxia Neuropathy Spectrum,Visual Pathway Disease,Childhood Myocerebrohepatopathy Spectrum,Myoclonic Epilepsy Myopathy Sensory Ataxia,Microcephaly,Dysphagia,Encephalopathy,Camptocormism,Mitochondrial Dna Depletion Syndrome 1,Bipolar Disorder,Autosomal Dominant Cerebellar Ataxia,Partial Motor Epilepsy,Fanconi Anemia, Complementation Group A,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 4,Mitochondrial Dna Depletion Syndrome 4b,Disease Of Mental Health,Unverricht-Lundborg Syndrome,Body Mass Index Quantitative Trait Locus 11,Lactic Acidosis,Dentatorubral-Pallidoluysian Atrophy,Multiple Sclerosis,Lennox-Gastaut Syndrome,Neonatal Period Electroclinical Syndrome,Mitochondrial Dna Depletion Syndrome 5,Early Infantile Epileptic Encephalopathy,Coenzyme Q10 Deficiency Disease,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Marinesco-Sjogren Syndrome,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Dna Depletion Syndrome 3,Mitochondrial Complex I Deficiency, Nuclear Type 1,Mitochondrial Dna Depletion Syndrome 4a,Ptosis,Pyruvate Dehydrogenase E1-Alpha Deficiency,Kearns-Sayre Syndrome,Leigh Syndrome,Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes,Myoclonic Epilepsy Associated With Ragged-Red Fibers,Neuropathy, Ataxia, And Retinitis Pigmentosa,Pearson Marrow-Pancreas Syndrome,Mitochondrial Dna Depletion Syndrome 6,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1,3-Methylglutaconic Aciduria, Type Iii,Epilepsy, Idiopathic Generalized,Phenylketonuria