homeobox D13 - CISMeF

Preferred Label : homeobox D13;

Approved symbol HGNC : HOXD13;

Name synonyms HGNC : synpolydactyly;

Chromosome HGNC : 2q31.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000128714;

Details

Origin ID

HGNC:5136;

UMLS CUI

C1415687;

Automatic exact mappings (from CISMeF team)
- Homeobox d13 [OMIM gene]
- Syndactyly type 2 [ICD-11 More detail]
- Syndactyly type 2 [ORDO Disease]
- Syndactyly type 2 (disorder) [SNOMED CT concept]
- Synpolydactyly [NCIt concept]
- homeobox D13 [ORDO Gene]
- syndactyly, type 2 [MeSH Supplementary Concept]
- synpolydactyly [DO Concept]
NCIt concept
- HOXD13 Gene [NCIt concept]
OMIM gene
- Homeobox d13 [OMIM gene]
Orphanet gene
- homeobox D13 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HOXD13 Gene [NCIt concept]
- Homeobox d13 [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients