Myosin viia - CISMeF

Preferred Label : Myosin viia;

Symbol : MYO7A;

CISMeF acronym : MYO7A;

Type : Gene;

Alternative titles and symbols : Myosin, unconventional, family VII, member a; MYU7A;

Ensembl ID : ENSG00000137474;

Prefixed ID : *276903;

Details

Origin ID

276903;

UMLS CUI

C1417569;

Automatic exact mappings (from CISMeF team)
- myosin VIIA [ORDO Gene]
- myosin VIIA [HGNC gene]
HGNC gene
- myosin VIIA [HGNC gene]
ORDO concept(s)
- myosin VIIA [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 11 [OMIM Phenotype]
- Deafness, autosomal recessive 2 [OMIM Phenotype]
- Usher syndrome, type I [OMIM Phenotype]
See also inter- (CISMeF)
- Myosin VIIa [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- myosin VIIA [HGNC gene]

Keyword's position in hierarchy(ies) :

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