ADP platelet receptor P2Y12 deficiency (Q84808)

Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss.

Language	Label	Description	Also known as
default for all languages	ID_121084770
English	ADP platelet receptor P2Y12 deficiency	Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss.