Coagulation Defects, Purpura And Other Hemorrhagic Conditions

(D65) Disseminated intravascular coagulation [defibrination syndrome]

(D66) Hereditary factor VIII deficiency

(D67) Hereditary factor IX deficiency

(D68) Other coagulation defects

(D68.0) Von Willebrand's disease

(D68.1) Hereditary factor XI deficiency

(D68.2) Hereditary deficiency of other clotting factors

(D68.3) Hemorrhagic disorder due to circulating anticoagulants

(D68.31) Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

(D68.311) Acquired hemophilia

(D68.312) Antiphospholipid antibody with hemorrhagic disorder

(D68.318) Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

(D68.32) Hemorrhagic disorder due to extrinsic circulating anticoagulants

(D68.4) Acquired coagulation factor deficiency

(D68.5) Primary thrombophilia

(D68.51) Activated protein C resistance

(D68.52) Prothrombin gene mutation

(D68.59) Other primary thrombophilia

(D68.6) Other thrombophilia

(D68.61) Antiphospholipid syndrome

(D68.62) Lupus anticoagulant syndrome

(D68.69) Other thrombophilia

(D68.8) Other specified coagulation defects

(D68.9) Coagulation defect, unspecified

(D69) Purpura and other hemorrhagic conditions