Mitochondrial myopathy with reversible cytochrome C oxidase deficiency 784370005
SNOMED CT code
| SNOMED code | 784370005 |
|---|---|
| name | Mitochondrial myopathy with reversible cytochrome C oxidase deficiency |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Mitochondrial myopathy 16851005 Mitochondrial myopathy with reversible cytochrome C oxidase deficiency 784370005 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Mitochondrial myopathy with reversible cytochrome C oxidase deficiency 784370005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Cytochrome-c oxidase deficiency 67434000 Mitochondrial myopathy with reversible cytochrome C oxidase deficiency 784370005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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