ICD-10-CM 2023: D60-D69

รหัสคำอธิบาย
D60Acquired pure red cell aplasia [erythroblastopenia]
D60.0Chronic acquired pure red cell aplasia
D60.1Transient acquired pure red cell aplasia
D60.8Other acquired pure red cell aplasias
D60.9Acquired pure red cell aplasia, unspecified
D61Other aplastic anemias and other bone marrow failure syndromes
D61.0Constitutional aplastic anemia
D61.01Constitutional (pure) red blood cell aplasia
D61.09Other constitutional aplastic anemia
D61.1Drug-induced aplastic anemia
D61.2Aplastic anemia due to other external agents
D61.3Idiopathic aplastic anemia
D61.8Other specified aplastic anemias and other bone marrow failure syndromes
D61.81Pancytopenia
D61.810Antineoplastic chemotherapy induced pancytopenia
D61.811Other drug-induced pancytopenia
D61.818Other pancytopenia
D61.82Myelophthisis
D61.89Other specified aplastic anemias and other bone marrow failure syndromes
D61.9Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D63Anemia in chronic diseases classified elsewhere
D63.0Anemia in neoplastic disease
D63.1Anemia in chronic kidney disease
D63.8Anemia in other chronic diseases classified elsewhere
D64Other anemias
D64.0Hereditary sideroblastic anemia
D64.1Secondary sideroblastic anemia due to disease
D64.2Secondary sideroblastic anemia due to drugs and toxins
D64.3Other sideroblastic anemias
D64.4Congenital dyserythropoietic anemia
D64.8Other specified anemias
D64.81Anemia due to antineoplastic chemotherapy
D64.89Other specified anemias
D64.9Anemia, unspecified
D65Disseminated intravascular coagulation [defibrination syndrome]
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D68Other coagulation defects
D68.0Von Willebrand disease
D68.00Von Willebrand disease, unspecified
D68.01Von Willebrand disease, type 1
D68.02Von Willebrand disease, type 2
D68.020Von Willebrand disease, type 2A
D68.021Von Willebrand disease, type 2B
D68.022Von Willebrand disease, type 2M
D68.023Von Willebrand disease, type 2N
D68.029Von Willebrand disease, type 2, unspecified
D68.03Von Willebrand disease, type 3
D68.04Acquired von Willebrand disease
D68.09Other von Willebrand disease
D68.1Hereditary factor XI deficiency
D68.2Hereditary deficiency of other clotting factors
D68.3Hemorrhagic disorder due to circulating anticoagulants
D68.31Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.311Acquired hemophilia
D68.312Antiphospholipid antibody with hemorrhagic disorder
D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4Acquired coagulation factor deficiency
D68.5Primary thrombophilia
D68.51Activated protein C resistance
D68.52Prothrombin gene mutation
D68.59Other primary thrombophilia
D68.6Other thrombophilia
D68.61Antiphospholipid syndrome
D68.62Lupus anticoagulant syndrome
D68.69Other 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
D69.41Evans syndrome
D69.42Congenital and hereditary thrombocytopenia purpura
D69.49Other primary thrombocytopenia
D69.5Secondary thrombocytopenia
D69.51Posttransfusion purpura
D69.59Other secondary thrombocytopenia
D69.6Thrombocytopenia, unspecified
D69.8Other specified hemorrhagic conditions
D69.9Hemorrhagic condition, unspecified