cardiomyopathy, familial hypertrophic, 6

Preferred Label : cardiomyopathy, familial hypertrophic, 6;

MeSH note : mutation in PRKAG2;

Origin ID

C563436;

UMLS CUI

C1833236;

Automatic exact mappings (from CISMeF team)
- hypertrophic cardiomyopathy 6 [DO Concept]
Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 6 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 6 [NCIt concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 6 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 6 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 6 [NCIt concept]