ICD-10-CM D50 to D89

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism: one chapter of ICD-10-CM.

398 codes · page 4 of 8 · every chapter

Other sideroblastic anemias D64.3 Congenital dyserythropoietic anemia D64.4 Other specified anemias D64.8 Anemia due to antineoplastic chemotherapy D64.81 Other specified anemias D64.89 Anemia, unspecified D64.9 Disseminated intravascular coagulation [defibrination syndrome] D65 Hereditary factor VIII deficiency D66 Hereditary factor IX deficiency D67 Other coagulation defects D68 Von Willebrand disease D68.0 Von Willebrand disease, unspecified D68.00 Von Willebrand disease, type 1 D68.01 Von Willebrand disease, type 2 D68.02 Von Willebrand disease, type 2A D68.020 Von Willebrand disease, type 2B D68.021 Von Willebrand disease, type 2M D68.022 Von Willebrand disease, type 2N D68.023 Von Willebrand disease, type 2, unspecified D68.029 Von Willebrand disease, type 3 D68.03 Acquired von Willebrand disease D68.04 Other von Willebrand disease D68.09 Hereditary factor XI deficiency D68.1 Hereditary deficiency of other clotting factors D68.2 Hemorrhagic disorder due to circulating anticoagulants D68.3 Hemorrhagic disorder due to intrns circ anticoag,antib,inhib Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors D68.31 Acquired hemophilia D68.311 Antiphospholipid antibody with hemorrhagic disorder D68.312 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors D68.318 Hemorrhagic disorder due to extrinsic circulating anticoagulants D68.32 Acquired coagulation factor deficiency D68.4 Primary thrombophilia D68.5 Activated protein C resistance D68.51 Prothrombin gene mutation D68.52 Other primary thrombophilia D68.59 Other thrombophilia D68.6 Antiphospholipid syndrome D68.61 Lupus anticoagulant syndrome D68.62 Other thrombophilia D68.69 Other specified coagulation defects D68.8 Coagulation defect, unspecified D68.9 Purpura and other hemorrhagic conditions D69 Allergic purpura D69.0 Qualitative platelet defects D69.1 Other nonthrombocytopenic purpura D69.2 Immune thrombocytopenic purpura D69.3 Other primary thrombocytopenia D69.4 Evans syndrome D69.41 Congenital and hereditary thrombocytopenia purpura D69.42 Other primary thrombocytopenia D69.49