D68.0   Von Willebrand's 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
D75.82   Heparin induced thrombocytopenia (HIT)
R23.3   Spontaneous ecchymoses