Myosin, heavy chain 7, cardiac muscle, beta

Preferred Label : Myosin, heavy chain 7, cardiac muscle, beta;

Symbol : MYH7;

CISMeF acronym : MYH7;

Type : Gene;

Alternative titles and symbols : Myosin, cardiac, heavy chain, beta; MYHCB;

Ensembl ID : ENSG00000092054;

Prefixed ID : *160760;

Détails

Origin ID

160760;

UMLS CUI

C1417542;

Automatic exact mappings (from CISMeF team)
- MYH7 gene [LOINC component]
- myosin heavy chain 7 [ORDO Gene]
- myosin heavy chain 7 [HGNC gene]
HGNC gene
- myosin heavy chain 7 [HGNC gene]
ORDO concept(s)
- myosin heavy chain 7 [ORDO Gene]
Phenotypes related
- Cardiomyopathy, dilated, 1s [OMIM Phenotype]
- Cardiomyopathy, familial hypertrophic, 1 [OMIM Phenotype]
- Congenital myopathy 7a, myosin storage, autosomal dominant [OMIM Phenotype]
- Congenital myopathy 7b, myosin storage, autosomal recessive [OMIM Phenotype]
- Myopathy, distal, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MYH7 gene [LOINC component]
- myosin heavy chain 7 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients