Ww domain-containing oxidoreductase

Preferred Label : Ww domain-containing oxidoreductase;

Symbol : WWOX;

CISMeF acronym : WWOX;

Type : Gene;

Alternative titles and symbols : Fragile site fra16d oxidoreductase; FOR; WOX1;

Included titles and symbols : Fragile site 16q23.2; FRA16D;

Ensembl ID : ENSG00000186153;

Prefixed ID : *605131;

Details

Origin ID

605131;

UMLS CUI

C1421525;

Automatic exact mappings (from CISMeF team)
- WW Domain-Containing Oxidoreductase [MeSH Descriptor]
- WW Domain-Containing Oxidoreductase [NCIt concept]
- WW domain containing oxidoreductase [ORDO Gene]
- WW domain containing oxidoreductase [HGNC gene]
- WWOX Gene [NCIt concept]
- WWOX wt Allele [NCIt concept]
HGNC gene
- WW domain containing oxidoreductase [HGNC gene]
NCIt concept(s)
- WW Domain-Containing Oxidoreductase [NCIt concept]
- WWOX Gene [NCIt concept]
- WWOX wt Allele [NCIt concept]
ORDO concept(s)
- WW domain containing oxidoreductase [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 28 [OMIM Phenotype]
- Esophageal cancer [OMIM Phenotype]
- Spinocerebellar ataxia, autosomal recessive 12 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WW domain containing oxidoreductase [HGNC gene]
- WWOX Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients