Hyperandrogenism due to cortisone reductase deficiency 783696009
SNOMED CT code
SNOMED code | 783696009 |
---|---|
name | Hyperandrogenism due to cortisone reductase deficiency |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Hyperandrogenism due to cortisone reductase deficiency (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Adrenal structure 23451007 |
attributes - group2 | |
Finding site | Gonadal endocrine structure 304041004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Hyperandrogenism due to cortisone reductase deficiency 783696009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of steroid metabolism 28710006 Hyperandrogenization syndrome 237793004 Hyperandrogenism due to cortisone reductase deficiency 783696009 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Adrenogenital disorder 267395000 Hyperandrogenism due to cortisone reductase deficiency 783696009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Hyperandrogenism due to cortisone reductase deficiency 783696009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Hyperandrogenism due to cortisone reductase deficiency 783696009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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