Claudin 19 - CISMeF

Preferred Label : Claudin 19;

Symbol : CLDN19;

CISMeF acronym : CLDN19;

Type : Gene;

Ensembl ID : ENSG00000164007;

Prefixed ID : *610036;

Details

Origin ID

610036;

UMLS CUI

C1413468;

Automatic exact mappings (from CISMeF team)
- claudin 19 [ORDO Gene]
- claudin 19 [HGNC gene]
HGNC gene
- claudin 19 [HGNC gene]
ORDO concept(s)
- claudin 19 [ORDO Gene]
Phenotypes related
- Hypomagnesemia 5, renal, with or without ocular involvement [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- claudin 19 [HGNC gene]

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