Autosomal recessive limb girdle muscular dystrophy type 2C 718176005
SNOMED CT code
SNOMED code | 718176005 |
---|---|
name | Autosomal recessive limb girdle muscular dystrophy type 2C |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dystrophy 4720007 |
Finding site | Skeletal muscle structure 127954009 |
attributes - group2 | |
Clinical course | Progressive 255314001 |
parents | Autosomal recessive muscular dystrophy with limb girdle distribution 240054004 |
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 recessive hereditary disorder 85995004 Autosomal recessive muscular dystrophy with limb girdle distribution 240054004 Autosomal recessive limb girdle muscular dystrophy type 2C 718176005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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