D65
Disseminated intravascular coagulation [defibrination syndrome]
Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
50 codes in this range
Disseminated intravascular coagulation [defibrination syndrome]
Hereditary factor VIII deficiency
Hereditary factor IX deficiency
Other coagulation defects
Von Willebrand disease
Von Willebrand disease, unspecified
Von Willebrand disease, type 1
Von Willebrand disease, type 2
Von Willebrand disease, type 2A
Von Willebrand disease, type 2B
Von Willebrand disease, type 2M
Von Willebrand disease, type 2N
Von Willebrand disease, type 2, unspecified
Von Willebrand disease, type 3
Acquired von Willebrand disease
Other von Willebrand disease
Hereditary factor XI deficiency
Hereditary deficiency of other clotting factors
Hemorrhagic disorder due to circulating anticoagulants
Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
Acquired hemophilia
Antiphospholipid antibody with hemorrhagic disorder
Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
Hemorrhagic disorder due to extrinsic circulating anticoagulants
Acquired coagulation factor deficiency
Primary thrombophilia
Activated protein C resistance
Prothrombin gene mutation
Other primary thrombophilia
Other thrombophilia
Antiphospholipid syndrome
Lupus anticoagulant syndrome
Other thrombophilia
Other specified coagulation defects
Coagulation defect, unspecified
Purpura and other hemorrhagic conditions
Allergic purpura
Qualitative platelet defects
Other nonthrombocytopenic purpura
Immune thrombocytopenic purpura
Other primary thrombocytopenia
Evans syndrome
Congenital and hereditary thrombocytopenia purpura
Other primary thrombocytopenia
Secondary thrombocytopenia
Posttransfusion purpura
Other secondary thrombocytopenia
Thrombocytopenia, unspecified
Other specified hemorrhagic conditions
Hemorrhagic condition, unspecified