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Nume Mitochondrial myopathy, not elsewhere classified
Pagina Web apps.who.int

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Boli A-Z Adenosine Monophosphate Deaminase 1 Deficiency Combined Oxidative Phosphorylation Deficiency 13 Combined Oxidative Phosphorylation Deficiency 24 Fastkd2-Related Infantile Mitochondrial Encephalomyopathy Fatal Infantile Cytochrome C Oxidase Deficiency Isolated Complex Iii Deficiency Mitochondrial Complex Ii Deficiency Mitochondrial Complex V Deficiency, Nuclear Type 2 Mitochondrial Dna Depletion Syndrome 11 Mitochondrial Dna Depletion Syndrome 2 Mitochondrial Dna Depletion Syndrome 5 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Myopathy, Infantile, Transient Mitochondrial Myopathy, Lethal, Infantile Mitochondrial Myopathy with Lactic Acidosis Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Phosphate Carrier Deficiency Mitochondrial Trifunctional Protein Deficiency Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy, Isolated Mitochondrial, Autosomal Dominant Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay Myopathy with Extrapyramidal Signs Myopathy with Lactic Acidosis, Hereditary Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 6 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 4 Pure Mitochondrial Myopathy Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis