Glycogen synthase deficiency 237964009
SNOMED CT code
| SNOMED code | 237964009 |
|---|---|
| name | Glycogen synthase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Glycogen synthase deficiency (disorder) |
| synonyms |
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| attributes - group2 | |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group1 | |
| Finding site | Liver structure 10200004 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| parents | |
| children | Hepatic glycogen synthase deficiency 725026008 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Glycogen synthase deficiency 237964009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Glycogen storage disease 29633007 Glycogen synthase deficiency 237964009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Glycogen synthase deficiency 237964009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Glycogen synthase deficiency 237964009 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Glycogen synthase deficiency 237964009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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