Congenital hypothyroidism due to symporter mutation 1179397005
SNOMED CT code
SNOMED code | 1179397005 |
---|---|
name | Congenital hypothyroidism due to symporter mutation |
status | active |
date introduced | 2021-11-30 |
fully specified name(s) | Congenital hypothyroidism due to symporter mutation (disorder) |
synonyms | Congenital hypothyroidism due to symporter mutation |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Thyroid structure 69748006 |
parents | Congenital hypothyroidism 190268003 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypothyroidism 190268003 Congenital hypothyroidism due to symporter mutation 1179397005 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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