Cytochrome p450, subfamily xib, polypeptide 2

Preferred Label : Cytochrome p450, subfamily xib, polypeptide 2;

Symbol : CYP11B2;

CISMeF acronym : CYP11B2;

Type : Gene;

Alternative titles and symbols : Steroid 11/18-beta-hydroxylase; Steroid 18-oxidase; Aldosterone synthase; ALDOS;

Included titles and symbols : Cmo I; Cmo II; Corticosterone methyloxidase II; Corticosterone methyloxidase I; Aldosterone to renin ratio, increased;

Ensembl ID : ENSG00000179142;

Prefixed ID : *124080;

Détails

Origin ID

124080;

UMLS CUI

C1413857;

Automatic exact mappings (from CISMeF team)
- CYP11B2 Gene [NCIt concept]
- CYP11B2 wt Allele [NCIt concept]
- Cytochrome P-450 CYP11B2 [MeSH concept]
- Cytochrome P-450 CYP11B2 [MeSH Descriptor]
- Cytochrome P450 11B2, Mitochondrial [NCIt concept]
- corticosterone methyl oxidase I [MeSH Supplementary Concept]
- corticosterone methyl oxidase II [MeSH Supplementary Concept]
- cytochrome P450 family 11 subfamily B member 2 [ORDO Gene]
- cytochrome P450 family 11 subfamily B member 2 [HGNC gene]
HGNC gene
- cytochrome P450 family 11 subfamily B member 2 [HGNC gene]
NCIt concept(s)
- CYP11B2 Gene [NCIt concept]
- CYP11B2 wt Allele [NCIt concept]
- Cytochrome P450 11B2, Mitochondrial [NCIt concept]
ORDO concept(s)
- cytochrome P450 family 11 subfamily B member 2 [ORDO Gene]
Phenotypes related
- Corticosterone methyloxidase type I deficiency [OMIM Phenotype]
- Corticosterone methyloxidase type II deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CYP11B2 Gene [NCIt concept]
- cytochrome P450 family 11 subfamily B member 2 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

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