cardiomyopathy, familial hypertrophic, 3

Preferred Label : cardiomyopathy, familial hypertrophic, 3;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566470;

UMLS CUI

C1861863;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 3 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 3 [NCIt concept]
- hypertrophic cardiomyopathy 3 [DO Concept]
Related record
- cardiomyopathy, familial hypertrophic, 3 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 3 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 3 [NCIt concept]