impaired adp-induced platelet aggregation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal platelet response to ADP as manifested by reduced or lacking aggregation of platelets upon addition of ADP. (Human Phenotype Ontology, HP_0004866)
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2 genes associated with the impaired adp-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HPS6 Hermansky-Pudlak syndrome 6
P2RY12 purinergic receptor P2Y, G-protein coupled, 12