| D68 | Other coagulation defects |
| | Von Willebrand’s disease |
| | Hereditary factor XI deficiency |
| | Hereditary deficiency of other clotting factors |
| | Hemorrhagic disorder due to circulating anticoagulants |
| | Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
| | Acquired hemophilia |
| | Antiphospholipid antibody with hemorrhagic disorder |
| | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
| | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
| | Acquired coagulation factor deficiency |
| | Primary thrombophilia |
| | Activated protein C resistance |
| | Prothrombin gene mutation |
| | Other primary thrombophilia |
| | Other thrombophilia |
| | Antiphospholipid syndrome |
| | Lupus anticoagulant syndrome |
| | Other thrombophilia |
| | Other specified coagulation defects |
| | Coagulation defect, unspecified |
