813 - Coagulation Disorders

• D68.00 - Von Willebrand disease, unspecified
• D68.01 - Von Willebrand disease, type 1
• D68.020 - Von Willebrand disease, type 2A
• D68.021 - Von Willebrand disease, type 2B
• D68.022 - Von Willebrand disease, type 2M
• D68.023 - Von Willebrand disease, type 2N
• D68.029 - Von Willebrand disease, type 2, unspecified
• D68.03 - Von Willebrand disease, type 3
• D68.04 - Acquired von Willebrand disease
• D68.09 - Other von Willebrand 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
• D69.6 - Thrombocytopenia, unspecified
• D69.8 - Other specified hemorrhagic conditions
• D69.9 - Hemorrhagic condition, unspecified
• R23.3 - Spontaneous ecchymoses