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Up to: Autosomal genetic disease · Hemorrhagic disease · Inherited blood coagulation disorder · Coagulation protein disease · Congenital hematological disorder
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.
This condition has no sub-types.