myosin heavy chain 6

Preferred Label : myosin heavy chain 6;

Approved symbol HGNC : MYH6;

Name synonyms HGNC : cardiomyopathy; hypertrophic 1;

Chromosome HGNC : 14q11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000197616;

Détails

Origin ID

HGNC:7576;

UMLS CUI

C1417541;

Automatic exact mappings (from CISMeF team)
- CARDIOMYOPATHY [WHO-ART Preferred Term]
- Cardiomyopathies [MedDRA High Level Term]
- Cardiomyopathy [LOINC component]
- Cardiomyopathy [ICD-11 Category]
- Cardiomyopathy [NCIt concept]
- Cardiomyopathy [ICD-10 category]
- Cardiomyopathy [MedDRA Preferred Term]
- Cardiomyopathy [ICD-9 code]
- Cardiomyopathy [PASCAL descriptor]
- Cardiomyopathy [HPO term]
- Cardiomyopathy (disorder) [SNOMED CT concept]
- Family History of Cardiomyopathy [NCIt concept]
- Myosin, heavy chain 6, cardiac muscle, alpha [OMIM gene]
- Rare cardiomyopathy [ORDO Disease]
- cardiomyopathies [MeSH Descriptor]
- cardiomyopathies [MeSH concept]
- cardiomyopathy [DO Concept]
- cardiomyopathy [MedlinePlus Topic]
- cardiomyopathy [Radlex concept]
- myosin heavy chain 6 [ORDO Gene]
NCIt concept
- MYH6 Gene [NCIt concept]
OMIM gene
- Myosin, heavy chain 6, cardiac muscle, alpha [OMIM gene]
Orphanet gene
- myosin heavy chain 6 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MYH6 Gene [NCIt concept]
- Myosin, heavy chain 6, cardiac muscle, alpha [OMIM gene]

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