Mitochondrial myopathies

ICD-11 code : 8C73;

Preferred Label : Mitochondrial myopathies;

ICD-11 definition : 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 fibers (MERRF);

ICD-11 synonym : Myopathies in mitochondrial disorders;

ICD-11 "other" category code : 8C73.Y;

ICD-11 "unspecified" category code : 8C73.Z;

Details

Origin ID

601991549;

Currated CISMeF NLP mapping
- Mitochondrial Myopathy [NCIt concept]
- Mitochondrial cytopathy (disorder) [SNOMED CT concept]
- Mitochondrial myopathy [HPO term]
- Mitochondrial myopathy [ORDO Disease]
- Mitochondrial myopathy [PASCAL descriptor]
- Mitochondrial myopathy [MedDRA Preferred Term]
- Mitochondrial myopathy (disorder) [SNOMED CT concept]
- Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathy [OMIM Phenotype]
- mitochondrial myopathies [MeSH Descriptor]
- mitochondrial myopathies [MeSH concept]
- mitochondrial myopathy [DO Concept]
- mitochondrial myopathy [SNOMED Notion]
ICD-10 Mapping
- Mitochondrial myopathy, not elsewhere classified [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

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