Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009
SNOMED CT code
| SNOMED code | 1222644009 |
|---|---|
| name | Autosomal dominant mitochondrial myopathy with exercise intolerance |
| status | active |
| date introduced | 2022-05-31 |
| fully specified name(s) | Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder) |
| synonyms | Autosomal dominant mitochondrial myopathy with exercise intolerance |
| attributes - group1 | |
| Clinical course | Progressive 255314001 |
| attributes - group2 | |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of musculoskeletal system 128237006 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic metabolic disorder 128289001 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Mitochondrial myopathy 16851005 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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