Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006
SNOMED CT code
SNOMED code | 717261006 |
---|---|
name | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) |
synonyms | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
attributes - group1 | |
Finding site | Adrenal cortex structure 68594002 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hyperplasia 76197007 |
attributes - group2 | |
Due to | Deficiency of steroid 21-monooxygenase 124221007 |
parents | Congenital adrenal hyperplasia 237751000 |
children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Congenital adrenal hyperplasia 237751000 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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