Claudin 14 - CISMeF

" /> Claudin 14 - CISMeF

CISMeF

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Claudin 14OMIM gene

Preferred Label : Claudin 14;

Symbol : CLDN14;

CISMeF acronym : CLDN14;

Type : Gene;

Ensembl ID : ENSG00000159261;

Prefixed ID : *605608;

Details

Origin ID

605608;

UMLS CUI

C1413463;

Automatic exact mappings (from CISMeF team)
- claudin 14 [ORDO Gene]
- claudin 14 [MeSH concept]
- claudin 14 [MeSH Supplementary Concept]
- claudin 14 [HGNC gene]
HGNC gene
- claudin 14 [HGNC gene]
ORDO concept(s)
- claudin 14 [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 29 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- claudin 14 [HGNC gene]

Keyword's position in hierarchy(ies) :

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07/05/2025

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