Informaţii despre
| Nume | | Mitochondrial myopathy, not elsewhere classified |
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| Pagina Web | | apps.who.int |
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Vezi şi
| 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 |
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