Autosomal dominant limb girdle muscular dystrophy type 1D 719987009
SNOMED CT code
SNOMED code | 719987009 |
---|---|
name | Autosomal dominant limb girdle muscular dystrophy type 1D |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) |
synonyms | Autosomal dominant limb girdle muscular dystrophy type 1D |
attributes - group1 | |
Finding site | Skeletal muscle structure 127954009 |
Associated morphology | Dystrophy 4720007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Clinical course | Progressive 255314001 |
parents | Autosomal dominant muscular dystrophy with limb girdle distribution 240067001 |
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 muscular dystrophy with limb girdle distribution 240067001 Autosomal dominant limb girdle muscular dystrophy type 1D 719987009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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