cardiomyopathy, familial hypertrophic, 10

Preferred Label : cardiomyopathy, familial hypertrophic, 10;

MeSH note : mutation in MYL2;

MeSH synonym : cardiomyopathy, hypertrophic, Mid-Left ventricular chamber type, 2;

Details

Origin ID

C563865;

UMLS CUI

C1834460;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 10 [OMIM Phenotype]
- hypertrophic cardiomyopathy 10 [DO Concept]
MeSH term(s) associated for indexing
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
Record concept(s)
- cardiomyopathy, familial hypertrophic, 10 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, familial hypertrophic, 10 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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