DRG 813 Coagulation disorders

Coagulation disorders

Coagulation disorders

D65  Disseminated intravascular coagulation [defibrination syndrome]

D66  Hereditary factor VIII deficiency

D67  Hereditary factor IX deficiency

D68.00  Von Willebrand disease, unspecified

D68.01  Von Willebrand disease, type 1

D68.020  Von Willebrand disease, type 2A

D68.021  Von Willebrand disease, type 2B

D68.022  Von Willebrand disease, type 2M

D68.023  Von Willebrand disease, type 2N

D68.029  Von Willebrand disease, type 2, unspecified

D68.03  Von Willebrand disease, type 3

D68.04  Acquired von Willebrand disease

D68.09  Other von Willebrand disease

D68.1  Hereditary factor XI deficiency

D68.2  Hereditary deficiency of other clotting factors

D68.311  Acquired hemophilia

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

D68.8  Other specified coagulation defects

D68.9  Coagulation defect, unspecified

D69.0  Allergic purpura

D69.1  Qualitative platelet defects

D69.2  Other nonthrombocytopenic purpura

D69.3  Immune thrombocytopenic purpura

D69.41  Evans syndrome

D69.42  Congenital and hereditary thrombocytopenia purpura

D69.49  Other primary thrombocytopenia

D69.51  Posttransfusion purpura

D69.59  Other secondary thrombocytopenia

D69.6  Thrombocytopenia, unspecified

D69.8  Other specified hemorrhagic conditions

D69.9  Hemorrhagic condition, unspecified

D75.821  Non-immune heparin-induced thrombocytopenia

D75.822  Immune-mediated heparin-induced thrombocytopenia

D75.828  Other heparin-induced thrombocytopenia syndrome

D75.829  Heparin-induced thrombocytopenia, unspecified

D75.84  Other platelet-activating anti-PF4 disorders

R23.3  Spontaneous ecchymoses