Integrin, alpha-7

Preferred Label : Integrin, alpha-7;

Symbol : ITGA7;

CISMeF acronym : ITGA7;

Type : Gene;

Ensembl ID : ENSG00000135424;

Prefixed ID : *600536;

Details

Origin ID

600536;

UMLS CUI

C1416489;

Automatic exact mappings (from CISMeF team)
- integrin alpha7 [MeSH concept]
- integrin alpha7 [MeSH Supplementary Concept]
- integrin alpha7beta1 [MeSH Supplementary Concept]
- integrin subunit alpha 7 [HGNC gene]
- integrin subunit alpha 7 [ORDO Gene]
HGNC gene
- integrin subunit alpha 7 [HGNC gene]
ORDO concept(s)
- integrin subunit alpha 7 [ORDO Gene]
Phenotypes related
- Muscular dystrophy, congenital, due to integrin alpha-7 deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- integrin subunit alpha 7 [HGNC gene]

Keyword's position in hierarchy(ies) :

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