Coagulation Disorders

Principal diagnosis codes (39)

• D65Disseminated intravascular coagulation [defibrination syndrome]
• D66Hereditary factor VIII deficiency
• D67Hereditary factor IX deficiency
• D68.00Von Willebrand disease, unspecified
• D68.01Von Willebrand disease, type 1
• D68.020Von Willebrand disease, type 2A
• D68.021Von Willebrand disease, type 2B
• D68.022Von Willebrand disease, type 2M
• D68.023Von Willebrand disease, type 2N
• D68.029Von Willebrand disease, type 2, unspecified
• D68.03Von Willebrand disease, type 3
• D68.04Acquired von Willebrand disease
• D68.09Other von Willebrand disease
• D68.1Hereditary factor XI deficiency
• D68.2Hereditary deficiency of other clotting factors
• D68.311Acquired hemophilia
• D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
• D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulants
• D68.4Acquired coagulation factor deficiency
• D68.8Other specified coagulation defects
• D68.9Coagulation defect, unspecified
• D69.0Allergic purpura
• D69.1Qualitative platelet defects
• D69.2Other nonthrombocytopenic purpura
• D69.3Immune thrombocytopenic purpura
• D69.41Evans syndrome
• D69.42Congenital and hereditary thrombocytopenia purpura
• D69.49Other primary thrombocytopenia
• D69.51Posttransfusion purpura
• D69.59Other secondary thrombocytopenia
• D69.6Thrombocytopenia, unspecified
• D69.8Other specified hemorrhagic conditions
• D69.9Hemorrhagic condition, unspecified
• D75.821Non-immune heparin-induced thrombocytopenia
• D75.822Immune-mediated heparin-induced thrombocytopenia
• D75.828Other heparin-induced thrombocytopenia syndrome
• D75.829Heparin-induced thrombocytopenia, unspecified
• D75.84Other platelet-activating anti-PF4 disorders
• R23.3Spontaneous ecchymoses