Distal-less homeobox 5

Preferred Label : Distal-less homeobox 5;

Symbol : DLX5;

CISMeF acronym : DLX5;

Type : Gene;

Ensembl ID : ENSG00000105880;

Prefixed ID : *600028;

Details

Origin ID

600028;

UMLS CUI

C1414079;

Automatic exact mappings (from CISMeF team)
- DLX5 Gene [NCIt concept]
- Homeobox Protein DLX-5 [NCIt concept]
- distal-less homeobox 5 [ORDO Gene]
- distal-less homeobox 5 [HGNC gene]
HGNC gene
- distal-less homeobox 5 [HGNC gene]
NCIt concept(s)
- DLX5 Gene [NCIt concept]
- DLX5 wt Allele [NCIt concept]
- Homeobox Protein DLX-5 [NCIt concept]
ORDO concept(s)
- distal-less homeobox 5 [ORDO Gene]
Phenotypes related
- Split-hand/foot malformation 1 [OMIM Phenotype]
- Split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DLX5 Gene [NCIt concept]
- distal-less homeobox 5 [HGNC gene]

Keyword's position in hierarchy(ies) :

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