Childhood-onset nemaline myopathy 1197154006
SNOMED CT code
| SNOMED code | 1197154006 |
|---|---|
| name | Childhood-onset nemaline myopathy |
| status | active |
| date introduced | 2022-02-28 |
| fully specified name(s) | Childhood-onset nemaline myopathy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Childhood 255398004 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| 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 Childhood-onset nemaline myopathy 1197154006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of musculoskeletal system 128237006 Childhood-onset nemaline myopathy 1197154006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Childhood-onset nemaline myopathy 1197154006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Nemaline myopathy 75072002 Childhood-onset nemaline myopathy 1197154006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com