| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A disorder of the cardiac conduction system of the heart characterized by ventricular preexcitation due to the presence of an abnormal accessory atrioventricular electrical conduction pathway. (Human Phenotype Ontology, HP_0001716) |
| External Link | http://www.omim.org/entry/194200 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PRKAG2 | protein kinase, AMP-activated, gamma 2 non-catalytic subunit |
