Myosin VI - CISMeF

Preferred Label : Myosin VI;

Symbol : MYO6;

CISMeF acronym : MYO6;

Type : Gene;

Ensembl ID : ENSG00000196586;

Prefixed ID : *600970;

Details

Origin ID

600970;

UMLS CUI

C1417568;

Automatic exact mappings (from CISMeF team)
- myosin VI [ORDO Gene]
- myosin VI [HGNC gene]
- myosin VI [MeSH Supplementary Concept]
- myosin VI [MeSH concept]
HGNC gene
- myosin VI [HGNC gene]
ORDO concept(s)
- myosin VI [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 22 [OMIM Phenotype]
- Deafness, autosomal recessive 37 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- myosin VI [HGNC gene]

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