Congenital factor XII deficiency

Congenital factor XII deficiency is an autosomal recessive systemic dysfunction of the hemostatic pathway, that is due to a defect in the coagulation factor XII (FXII or Hageman factor), and is either asymptomatic or characterized by a prolonged activated partial thromboplastin time and an increased risk for thromboembolism. FXII deficiency is strongly associated with primary recurrent abortions.

Also known as: Factor XII Deficiency, Hageman Factor deficiency, congenital Hageman factor deficiency, congenital factor XII deficiency, F12 deficiency, Haf deficiency, coagulation factor 12 deficiency, factor 12 deficiency

13 clinical trials for this condition and its sub-types, 1 tagged with Congenital factor XII deficiency itself.