|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormal response to thrombin or thrombin mimetics as manifested by reduced or lacking aggregation of platelets upon addition of thrombin (or thrombin mimetics). (Human Phenotype Ontology, HP_0011872)|
|Downloads & Tools|
1 genes associated with the impaired thrombin-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.