Cytochrome p450, family 17, subfamily a, polypeptide 1

Preferred Label : Cytochrome p450, family 17, subfamily a, polypeptide 1;

Symbol : CYP17A1;

CISMeF acronym : CYP17A1;

Type : Gene;

Alternative titles and symbols : Steroid 17-alpha-monooxygenase; Cytochrome p450, subfamily XVII; Steroid 17-hydroxylase/17,20-lyase; CYP17; P450C17; S17AH;

Ensembl ID : ENSG00000148795;

Prefixed ID : *609300;

Details

Origin ID

609300;

UMLS CUI

C1413858;

Automatic exact mappings (from CISMeF team)
- CYP17A1 Gene [NCIt concept]
- CYP17A1 gene [LOINC component]
- CYP17A1 wt Allele [NCIt concept]
- Steroid 17-Alpha-Hydroxylase/17,20 Lyase [NCIt concept]
- Steroid 17-alpha-monooxygenase (substance) [SNOMED CT concept]
- cytochrome P450 family 17 subfamily A member 1 [ORDO Gene]
- cytochrome P450 family 17 subfamily A member 1 [HGNC gene]
- steroid 17-alpha-hydroxylase [MeSH Descriptor]
- steroid 17-alpha-monooxygenase [SNOMED Notion]
HGNC gene
- cytochrome P450 family 17 subfamily A member 1 [HGNC gene]
NCIt concept(s)
- CYP17A1 Gene [NCIt concept]
- CYP17A1 wt Allele [NCIt concept]
- Steroid 17-Alpha-Hydroxylase/17,20 Lyase [NCIt concept]
ORDO concept(s)
- cytochrome P450 family 17 subfamily A member 1 [ORDO Gene]
Phenotypes related
- Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CYP17A1 Gene [NCIt concept]
- CYP17A1 gene [LOINC component]
- cytochrome P450 family 17 subfamily A member 1 [HGNC gene]

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