Conditions / Genetic

antithrombin III deficiency

info · Genetic · ICD-10: D68.59

A thrombophilia that is characterized by the tendency to form clots in the veins.

Signs and symptoms

  • Decreased level of heparin co-factor II
  • Recurrent thrombophlebitis
  • Arterial occlusion
  • Reduced antithrombin III activity
  • Deep venous thrombosis
  • Cerebral venous thrombosis
  • Pulmonary embolism

Medications that may treat it

antithrombin III estrogens, conjugated (USP) estrone

Also known as: AT III deficiency; hereditary thrombophilia due to congenital antithrombin deficiency