mild steroid 21-hydroxylase deficiency

Preferred Label : mild steroid 21-hydroxylase deficiency;

Origin ID

D6-80142;

UMLS CUI

C0268288;

Currated CISMeF NLP mapping
- Mild steroid 21-hydroxylase deficiency (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Congenital adrenogenital disorders associated with enzyme deficiency [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- steroid 21-monooxygenase [SNOMED Notion]
SNOMED CT concept
- Mild steroid 21-hydroxylase deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mild steroid 21-hydroxylase deficiency (disorder) [SNOMED CT concept]