MDC 16 Diseases & Disorders of Blood, Blood Forming Organs, Immunologic Disorders |
Coagulation Disorders |
D65 | Disseminated intravascular coagulation [defibrination syndrome] |
D66 | Hereditary factor VIII deficiency |
D67 | Hereditary factor IX deficiency |
D680 | Von Willebrand's disease |
D681 | Hereditary factor XI deficiency |
D682 | Hereditary deficiency of other clotting factors |
D68311 | Acquired hemophilia |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7582 | Heparin induced thrombocytopenia (HIT) |
R233 | Spontaneous ecchymoses |