|Dataset||GWASdb SNP-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. (Human Disease Ontology, DOID_11984)|
|Downloads & Tools|
5 genes associated with the hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.