Homeobox a13 - CISMeF

Preferred Label : Homeobox a13;

Symbol : HOXA13;

CISMeF acronym : HOXA13;

Type : Gene;

Alternative titles and symbols : Homeobox 1j; HOX1J;

Ensembl ID : ENSG00000106031;

Prefixed ID : *142959;

Details

Origin ID

142959;

UMLS CUI

C1415655;

Automatic exact mappings (from CISMeF team)
- HOXA13 Gene [NCIt concept]
- HOXA13 wt Allele [NCIt concept]
- Homeobox Protein Hox-A13 [NCIt concept]
- homeobox A13 [ORDO Gene]
- homeobox A13 [HGNC gene]
HGNC gene
- homeobox A13 [HGNC gene]
NCIt concept(s)
- HOXA13 Gene [NCIt concept]
- HOXA13 wt Allele [NCIt concept]
- Homeobox Protein Hox-A13 [NCIt concept]
ORDO concept(s)
- homeobox A13 [ORDO Gene]
Phenotypes related
- Hand-foot-genital syndrome [OMIM Phenotype]
- Preaxial deficiency, postaxial polydactyly, and hypospadias [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HOXA13 Gene [NCIt concept]
- homeobox A13 [HGNC gene]

Keyword's position in hierarchy(ies) :

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