Myosin, heavy chain 9, nonmuscle

Preferred Label : Myosin, heavy chain 9, nonmuscle;

Symbol : MYH9;

CISMeF acronym : MYH9;

Type : Gene;

Alternative titles and symbols : Cellular myosin heavy chain, type a; Myosin, heavy chain, nonmuscle, type a; Nonmuscle myosin iia; Nmhc iia; NMMHCA;

Ensembl ID : ENSG00000100345;

Prefixed ID : *160775;

Details

Origin ID

160775;

UMLS CUI

C1417544;

Automatic exact mappings (from CISMeF team)
- MYH9 Gene [NCIt concept]
- MYH9 wt Allele [NCIt concept]
- Myosin-9 [NCIt concept]
- myosin heavy chain 9 [ORDO Gene]
- myosin heavy chain 9 [HGNC gene]
HGNC gene
- myosin heavy chain 9 [HGNC gene]
NCIt concept(s)
- MYH9 Gene [NCIt concept]
- MYH9 wt Allele [NCIt concept]
- Myosin-9 [NCIt concept]
ORDO concept(s)
- myosin heavy chain 9 [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 17 [OMIM Phenotype]
- Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MYH9 Gene [NCIt concept]
- myosin heavy chain 9 [HGNC gene]

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