congenital factor XII deficiency

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Disease Overview

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.


Synonyms

  • F12 deficiency
  • Factor XII Deficiency
  • Haf deficiency
  • Hageman Factor deficiency
  • coagulation factor 12 deficiency
  • congenital Hageman factor deficiency
  • congenital factor XII deficiency
  • deficiency, Hageman
  • factor 12 deficiency
  • factor XII deficiency
  • factor XII deficiency diseaseF12 deficiency
  • Factor XII Deficiency
  • Haf deficiency
  • Hageman Factor deficiency
  • coagulation factor 12 deficiency
  • congenital Hageman factor deficiency
  • congenital factor XII deficiency
  • deficiency, Hageman
  • factor 12 deficiency
  • factor XII deficiency
  • factor XII deficiency disease