| Dataset | GWASdb SNP-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. (Human Disease Ontology, DOID_11984) |
| 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.
