D50–D89: Diseases of the Blood and Blood-Forming Organs
Chapter 3 of ICD-10-CM 2027, 403 codes in 7 blocks.
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Chapter instructions
Excludes2: not included here, code separately if applicable
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Codes in this chapter
All codesBillable only403 results
- 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
- D69.11Glanzmann thrombasthenia
- D69.19Other qualitative platelet defects
- D69.2Other nonthrombocytopenic purpura
- D69.3Immune thrombocytopenic purpura
- D69.4Other primary thrombocytopenia
- D69.41Evans syndrome