cardiomyopathy, familial hypertrophic, 2

Preferred Label : cardiomyopathy, familial hypertrophic, 2;

Origin ID

C566171;

UMLS CUI

C1861864;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 2 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 2 [NCIt concept]
- hypertrophic cardiomyopathy 2 [DO Concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
- troponin t [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 2 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 2 [NCIt concept]
- hypertrophic cardiomyopathy 2 [DO Concept]