DRG 813

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