Mitochondrial Encephalomyopathy,Myopathy,Overnutrition,Basal Ganglia Disease,Neurodegeneration With Brain Iron Accumulation,Peripheral Vascular Disease,Leukoregulin,Neurodegeneration With Brain Iron Accumulation 8,Immune Deficiency Disease,Carnitine Acetyltransferase Deficiency,Carnitine Palmitoyltransferase I Deficiency,Leigh Syndrome,Carnitine Palmitoyltransferase Ii Deficiency, Infantile

Megacolon,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Central Sleep Apnea,Neuromuscular Junction Disease,Neuromuscular Disease,Congenital Myasthenic Syndrome Associated With Acetylcholine Receptor Deficiency,Congenital Myasthenic Syndrome With Episodic Apnea,Alzheimer Disease,Constipation,Amyotrophic Lateral Sclerosis 1,Mild Cognitive Impairment,Motor Neuron Disease,Neuroblastoma,Myasthenic Syndrome, Congenital, 21, Presynaptic,Apnea, Central Sleep,Riboflavin Deficiency,Chronic Progressive External Ophthalmoplegia,Neurotic Disorder,Presynaptic Congenital Myasthenic Syndromes,Ocular Dominance,Gastroesophageal Reflux,Sudden Infant Death Syndrome,Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Dementia,Scrapie,Vascular Dementia,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 1, Autosomal Dominant,Febrile Seizures,Head Injury,Amnestic Disorder,Pick Disease Of Brain,Wernicke-Korsakoff Syndrome,Central Nervous System Disease,Respiratory Failure,Tendinosis,Olivopontocerebellar Atrophy,Cone-Rod Dystrophy 2,Disease Of Mental Health,Toxic Encephalopathy,Congenital Myasthenic Syndrome,Lactic Acidosis,Retinitis Pigmentosa 23,Generalized Epilepsy With Febrile Seizures Plus, Type 7,Dementia, Lewy Body,Schizophrenia,Aspiration Pneumonia,Down Syndrome,Vertical Talus, Congenital,Huntington Disease,Cataract 38,Multiple System Atrophy 1,Myasthenic Syndrome, Congenital, 19,Ptosis,Rett Syndrome,Myasthenic Syndrome, Congenital, 6, Presynaptic,Thiamine Deficiency Disease