| Dataset | GWASdb SNP-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://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001639 |
| Similar Terms | |
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5 genes associated with the hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
