Amish nemaline myopathy 1197155007
SNOMED CT code
| SNOMED code | 1197155007 |
|---|---|
| name | Amish nemaline myopathy |
| status | active |
| date introduced | 2022-02-28 |
| fully specified name(s) | Amish nemaline myopathy (disorder) |
| synonyms | Amish nemaline myopathy |
| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Nemaline myopathy, early onset type 129621001 Amish nemaline myopathy 1197155007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Amish nemaline myopathy 1197155007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Amish nemaline myopathy 1197155007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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