steroid 21-monooxygenase deficiency, salt wasting type - CISMeF

" /> steroid 21-monooxygenase deficiency, salt wasting type - CISMeF

CISMeF

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Steroid 21-monooxygenase deficiency, salt wasting typeSNOMED Notion

Preferred Label : steroid 21-monooxygenase deficiency, salt wasting type;

Details

Origin ID

D6-80150;

UMLS CUI

C0268291;

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
- Steroid 21-monooxygenase deficiency, salt wasting type (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- 21 hydroxylase deficiency with salt wasting [Disease (Nov.)]
- Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form [ORDO Disease]
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, classic form, salt wasting [ICD-11 More detail]
- Steroid 21-monooxygenase deficiency, salt wasting type (disorder) [SNOMED CT concept]

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01/05/2025

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