Cytochrome p450, family 21, subfamily a, polypeptide 2

Preferred Label : Cytochrome p450, family 21, subfamily a, polypeptide 2;

Symbol : CYP21A2;

CISMeF acronym : CYP21A2;

Type : Gene;

Alternative titles and symbols : Cytochrome p450, subfamily xxia, polypeptide 2; Cytochrome p450, subfamily XXI; Steroid cytochrome p450 21-hydroxylase; 21-hydroxylase b; CYP21; P450C21; CYP21B; CA21H;

Included titles and symbols : Cytochrome p450, subfamily xxia, polypeptide 1 pseudogene; Cyp21p; CYP21A1P; CYP21A;

Ensembl ID : ENSG00000231852;

Prefixed ID : *613815;

Details

Origin ID

613815;

UMLS CUI

C1413861;

Automatic exact mappings (from CISMeF team)
- CYP21A2 Gene [NCIt concept]
- CYP21A2 gene [LOINC component]
- CYP21A2 wt Allele [NCIt concept]
- Cytochrome p450 CYP21A2 enzyme (substance) [SNOMED CT concept]
- 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]
HGNC gene
- cytochrome P450 family 21 subfamily A member 2 [HGNC gene]
NCIt concept(s)
- CYP21A2 Gene [NCIt concept]
- CYP21A2 wt Allele [NCIt concept]
- Steroid 21-Hydroxylase [NCIt concept]
ORDO concept(s)
- cytochrome P450 family 21 subfamily A member 2 [ORDO Gene]
Phenotypes related
- Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CYP21A2 Gene [NCIt concept]
- CYP21A2 gene [LOINC component]
- cytochrome P450 family 21 subfamily A member 2 [HGNC gene]

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