cardiomyopathy, familial hypertrophic, 1

Preferred Label : cardiomyopathy, familial hypertrophic, 1;

MeSH note : promote to HM;

Origin ID

C566005;

UMLS CUI

C3495498;

Currated CISMeF NLP mapping
- Asymmetric septal hypertrophy [HPO term]
- Asymmetrical septal hypertrophy [ICD-11 More detail]
- Cardiomyopathy, familial hypertrophic, 1 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 1 [NCIt concept]
- hypertrophic cardiomyopathy 1 [DO Concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 1 [OMIM Phenotype]
- Familial Hypertrophic Cardiomyopathy Type 1 [NCIt concept]
- hypertrophic cardiomyopathy 1 [DO Concept]