D65-D69
Coagulation defects, purpura and other haemorrhagic conditions
- D65Disseminated intravascular coagulation [defibrination syndrome]
- D66Hereditary factor VIII deficiency
- D67Hereditary factor IX deficiency
- D68.0Von Willebrand's disease
- D68.1Hereditary factor XI deficiency
- D68.2Hereditary deficiency of other clotting factors
- D68.3Haemorrhagic disorder due to circulating anticoagulants
- D68.4Acquired coagulation factor deficiency
- D68.5Primary Thrombophilia
- D68.6Other Thrombophilia
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D69.0Allergic purpura
- D69.1Qualitative platelet defects
- D69.2Other nonthrombocytopenic purpura
- D69.3Idiopathic thrombocytopenic purpura
- D69.4Other primary thrombocytopenia
- D69.5Secondary thrombocytopenia
- D69.6Thrombocytopenia, unspecified
- D69.8Other specified haemorrhagic conditions
- D69.9Haemorrhagic condition, unspecified