Occludin - CISMeF

Preferred Label : Occludin;

Symbol : OCLN;

CISMeF acronym : OCLN;

Type : Gene;

Ensembl ID : ENSG00000197822;

Prefixed ID : *602876;

Details

Origin ID

602876;

UMLS CUI

C1417928;

Automatic exact mappings (from CISMeF team)
- occludin [ORDO Gene]
- occludin [MeSH concept]
- occludin [MeSH Descriptor]
- occludin [HGNC gene]
HGNC gene
- occludin [HGNC gene]
ORDO concept(s)
- occludin [ORDO Gene]
Phenotypes related
- Pseudo-torch syndrome 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- occludin [HGNC gene]

Keyword's position in hierarchy(ies) :

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