cardiomyopathy, familial hypertrophic, 11

Preferred Label : cardiomyopathy, familial hypertrophic, 11;

MeSH note : mutations in ACTC1;

Origin ID

C567419;

UMLS CUI

C2677506;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 11 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 11 [NCIt concept]
- hypertrophic cardiomyopathy 11 [DO Concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 11 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 11 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 11 [NCIt concept]