Hypertrophic cardiomyopathy Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY).|A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract. (Experimental Factor Ontology, EFO_0000538)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=CN001492
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Genes

1 genes associated with the Hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MYOM1 myomesin 1