Nuclear receptor subfamily 0, group b, member 1

Preferred Label : Nuclear receptor subfamily 0, group b, member 1;

Symbol : NR0B1;

CISMeF acronym : NR0B1;

Type : Gene;

Alternative titles and symbols : Dss-ahc critical region on the X chromosome 1, gene 1; DAX1;

Ensembl ID : ENSG00000169297;

Prefixed ID : *300473;

Details

Origin ID

300473;

UMLS CUI

C1417820;

Automatic exact mappings (from CISMeF team)
- DAX-1 orphan nuclear receptor [MeSH Descriptor]
- NR0B1 Gene [NCIt concept]
- NR0B1 gene [LOINC component]
- NR0B1 wt Allele [NCIt concept]
- Nuclear Receptor Subfamily 0 Group B Member 1 [NCIt concept]
- nuclear receptor subfamily 0 group B member 1 [ORDO Gene]
- nuclear receptor subfamily 0 group B member 1 [HGNC gene]
HGNC gene
- nuclear receptor subfamily 0 group B member 1 [HGNC gene]
NCIt concept(s)
- NR0B1 Gene [NCIt concept]
- NR0B1 wt Allele [NCIt concept]
- Nuclear Receptor Subfamily 0 Group B Member 1 [NCIt concept]
ORDO concept(s)
- nuclear receptor subfamily 0 group B member 1 [ORDO Gene]
Phenotypes related
- 46,xy sex reversal 2 [OMIM Phenotype]
- Adrenal hypoplasia, congenital [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NR0B1 Gene [NCIt concept]
- NR0B1 gene [LOINC component]
- nuclear receptor subfamily 0 group B member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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