steroid 21-monooxygenase - CISMeF

" /> steroid 21-monooxygenase - CISMeF

CISMeF

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Steroid 21-monooxygenaseSNOMED Notion

Preferred Label : steroid 21-monooxygenase;

Details

Origin ID

F-67488;

UMLS CUI

C0038304;

Automatic exact mappings (from CISMeF team)
- Steroid 21-Hydroxylase [NCIt concept]
- cytochrome P450 family 21 subfamily A member 2 [ORDO Gene]
- cytochrome P450 family 21 subfamily A member 2 [HGNC gene]
- steroid 21-Hydroxylase [MeSH concept]
- steroid 21-hydroxylase [MeSH Descriptor]
Currated CISMeF NLP mapping
- Steroid 21-monooxygenase (substance) [SNOMED CT concept]
Décrit
- mild steroid 21-hydroxylase deficiency [SNOMED Notion]
- moderate steroid 21-hydroxylase deficiency [SNOMED Notion]
- severe steroid 21-hydroxylase deficiency [SNOMED Notion]
- steroid 21-monooxygenase deficiency, salt wasting type [SNOMED Notion]
- steroid 21-monooxygenase deficiency, simple virilizing type [SNOMED Notion]
SNOMED CT concept
- Steroid 21-monooxygenase (substance) [SNOMED CT concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- 21-Hydroxylase [LOINC component]
- Steroid 21-monooxygenase (substance) [SNOMED CT concept]
- steroid 21-Hydroxylase [MeSH concept]
- steroid 21-hydroxylase [MeSH Descriptor]

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11/06/2024

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