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Nume Mitochondrial Dna-Associated Leigh Syndrome and Narp
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Boli A-Z 3-Methylglutaconic Aciduria, Type V Alzheimer Disease Mitochondrial Cercarial Dermatitis Chronic Progressive External Ophthalmoplegia Cortical Blindness Cranial Nerve Disease Cystic Echinococcosis Diabetes and Deafness, Maternally Inherited Diphyllobothriasis Early Myoclonic Encephalopathy Echinococcosis Encephalomyopathy Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Maternally-Inherited Progressive External Ophthalmoplegia Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy, Lactic Acidosis, and Sideroblastic Anemia Neuropathy, Ataxia, and Retinitis Pigmentosa Optic Nerve Disease Parkinson Disease 6, Autosomal Recessive Early-Onset Sparganosis Sudden Infant Death Syndrome
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