MS-DRG 813

Principal Diagnosis - Pdx

• 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