Polyglucosan body myopathy type 2 1228849007
SNOMED CT code
| SNOMED code | 1228849007 |
|---|---|
| name | Polyglucosan body myopathy type 2 |
| status | active |
| date introduced | 2022-05-31 |
| fully specified name(s) | Polyglucosan body myopathy type 2 (disorder) |
| synonyms |
|
| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of musculoskeletal system 128237006 Polyglucosan body myopathy type 2 1228849007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic metabolic disorder 128289001 Polyglucosan body myopathy type 2 1228849007 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Metabolic myopathy 26111005 Polyglucosan body myopathy type 2 1228849007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Glycogen storage disease 29633007 Polyglucosan body myopathy type 2 1228849007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Polyglucosan body myopathy type 2 1228849007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Polyglucosan body myopathy type 2 1228849007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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