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 only324 results
- D60.8Other acquired pure red cell aplasias
- D60.9Acquired pure red cell aplasia, unspecified
- D61.01Constitutional (pure) red blood cell aplasia
- D61.02Shwachman-Diamond syndrome
- D61.03Fanconi anemia
- D61.09Other constitutional aplastic anemia
- D61.1Drug-induced aplastic anemia
- D61.2Aplastic anemia due to other external agents
- D61.3Idiopathic aplastic anemia
- 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
- D63.0Anemia in neoplastic disease
- D63.1Anemia in chronic kidney disease
- D63.8Anemia in other chronic diseases classified elsewhere
- 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
- D64.81Anemia due to antineoplastic chemotherapy
- D64.89Other specified anemias
- D64.9Anemia, unspecified
- D65Disseminated intravascular coagulation [defibrination syndrome]
- D66Hereditary factor VIII deficiency
- D67Hereditary factor IX deficiency
- D68.00Von Willebrand disease, unspecified
- D68.01Von Willebrand disease, type 1
- 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
- D68.311Acquired 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
- D68.51Activated protein C resistance
- D68.52Prothrombin gene mutation
- D68.59Other primary thrombophilia