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