Mitochondrial myopathies (Q41402): Difference between revisions
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Latest revision as of 07:33, 13 August 2026
Mitochondrial myopathies are heterogeneous group of disorders caused by dysfunction of mitochondrial oxidative phosphorylation and can be classified according to the associated biochemical, genetic defects (in the mitochondrial DNA or in nuclear encoded proteins) or clinical phenotype. Exclude: defects of mitochondrial respiratory chain, Kearns-Sayre syndrome, myoclonic epilepsy with ragged red fibres (MERRF)
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C73 |
||
| English | Mitochondrial myopathies |
Mitochondrial myopathies are heterogeneous group of disorders caused by dysfunction of mitochondrial oxidative phosphorylation and can be classified according to the associated biochemical, genetic defects (in the mitochondrial DNA or in nuclear encoded proteins) or clinical phenotype. Exclude: defects of mitochondrial respiratory chain, Kearns-Sayre syndrome, myoclonic epilepsy with ragged red fibres (MERRF) |
Statements
CID11:8C73
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dki-india-8C73
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Concluído
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13 August 2026
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