Homeobox d13 - CISMeF

Preferred Label : Homeobox d13;

Symbol : HOXD13;

CISMeF acronym : HOXD13;

Type : Gene;

Alternative titles and symbols : Homeobox 4i; HOX4I;

Ensembl ID : ENSG00000128714;

Prefixed ID : *142989;

Details

Origin ID

142989;

UMLS CUI

C1415687;

Automatic exact mappings (from CISMeF team)
- HOXD13 Gene [NCIt concept]
- HOXD13 wt Allele [NCIt concept]
- Homeobox Protein Hox-D13 [NCIt concept]
- homeobox D13 [ORDO Gene]
- homeobox D13 [HGNC gene]
HGNC gene
- homeobox D13 [HGNC gene]
NCIt concept(s)
- HOXD13 Gene [NCIt concept]
- HOXD13 wt Allele [NCIt concept]
- Homeobox Protein Hox-D13 [NCIt concept]
ORDO concept(s)
- homeobox D13 [ORDO Gene]
Phenotypes related
- Brachydactyly, type D [OMIM Phenotype]
- Brachydactyly, type e1 [OMIM Phenotype]
- Brachydactyly-syndactyly syndrome [OMIM Phenotype]
- Syndactyly, type V [OMIM Phenotype]
- Synpolydactyly 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HOXD13 Gene [NCIt concept]
- homeobox D13 [HGNC gene]

Keyword's position in hierarchy(ies) :

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