cardiomyopathy, familial hypertrophic, 15

Preferred Label : cardiomyopathy, familial hypertrophic, 15;

Origin ID

C567681;

UMLS CUI

C2750459;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 15 [OMIM Phenotype]
- hypertrophic cardiomyopathy 15 [DO Concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
- vinculin [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 15 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 15 [OMIM Phenotype]