Congenital plasminogen activator inhibitor type 1 deficiency

Congenital plasminogen activator inhibitor type 1 (PAI-1) deficiency is a rare genetic bleeding disorder characterized by premature lysis of hemostatic clots and a moderate bleeding tendency.

Also known as: congenital PAI-1 deficiency, congenital plasminogen activator inhibitor type 1 deficiency, hyperfibrinolysis due to Pai1 deficiency, plasminogen activator INHIBITOR-1 deficiency, plasminogen activator inhibitor type 1 deficiency

47 clinical trials for this condition and its sub-types.