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familial hypertrophic cardiomyopathy

Disease Summary
Associated Targets (145)
Tbio

91

Tclin

27

Tchem

25

Tdark

2


GARD Rare
Mondo Description Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.
Disease Ontology Description A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.
Mondo Term and Equivalent IDs
MONDO:0024573:  familial hypertrophic cardiomyopathy
GARD:0007229: 
MESH:D024741: 
NCIT:C84773: 
OMIMPS:192600: 
SCTID:471885006: