ICD-10-CM 2027 · D65-D69
Coagulation defects, purpura and other hemorrhagic conditions
Part of chapter 3, diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
About D65-D69
D65Disseminated intravascular coagulation [defibrination syndrome]
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D68Other coagulation defects
- D68.0Von Willebrand disease
- D68.1Hereditary factor XI deficiency
- D68.2Hereditary deficiency of other clotting factors
- D68.3Hemorrhagic 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
D69Purpura and other hemorrhagic conditions
- D69.0Allergic purpura
- D69.1Qualitative platelet defects
- D69.2Other nonthrombocytopenic purpura
- D69.3Immune thrombocytopenic purpura
- D69.4Other primary thrombocytopenia
- D69.5Secondary thrombocytopenia
- D69.6Thrombocytopenia, unspecified
- D69.8Other specified hemorrhagic conditions
- D69.9Hemorrhagic condition, unspecified