ICD-10-CM
Diseases of the blood and blood-forming organs
Chapter 3, D50-D89. CDC FY2027 file dated June 16, 2026.
License. US government work, Public Domain Mark 1.0.
Categories
35 categories in this chapter. Open one, or page through every code below.
- D50Iron deficiency anemia
- D51Vitamin B12 deficiency anemia
- D52Folate deficiency anemia
- D53Other nutritional anemias
- D55Anemia due to enzyme disorders
- D56Thalassemia
- D57Sickle-cell disorders
- D58Other hereditary hemolytic anemias
- D59Acquired hemolytic anemia
- D60Acquired pure red cell aplasia [erythroblastopenia]
- D61Other aplastic anemias and other bone marrow failure syndromes
- D62Acute posthemorrhagic anemia
- D63Anemia in chronic diseases classified elsewhere
- D64Other anemias
- D65Disseminated intravascular coagulation
- D66Hereditary factor VIII deficiency
- D67Hereditary factor IX deficiency
- D68Other coagulation defects
- D69Purpura and other hemorrhagic conditions
- D70Neutropenia
- D71Functional disorders of polymorphonuclear neutrophils
- D72Other disorders of white blood cells
- D73Diseases of spleen
- D74Methemoglobinemia
- D75Other and unspecified diseases of blood and blood-forming organs
- D76Other dis with lymphoreticular and reticulohistiocytic tissue
- D77Other disord of bld/bld-frm organs in diseases classd elswhr
- D78Intraop and postprocedural complications of the spleen
- D80Immunodeficiency with predominantly antibody defects
- D81Combined immunodeficiencies
- D82Immunodeficiency associated with other major defects
- D83Common variable immunodeficiency
- D84Other immunodeficiencies
- D86Sarcoidosis
- D89Other disorders involving the immune mechanism, NEC
Codes
A header groups codes and is not billed. A billable code is one you can report.
161 to 200 of 403
- D68.0Von Willebrand diseaseHeader
- D68.00Von Willebrand disease, unspecifiedBillable
- D68.01Von Willebrand disease, type 1Billable
- D68.02Von Willebrand disease, type 2Header
- D68.020Von Willebrand disease, type 2ABillable
- D68.021Von Willebrand disease, type 2BBillable
- D68.022Von Willebrand disease, type 2MBillable
- D68.023Von Willebrand disease, type 2NBillable
- D68.029Von Willebrand disease, type 2, unspecifiedBillable
- D68.03Von Willebrand disease, type 3Billable
- D68.04Acquired von Willebrand diseaseBillable
- D68.09Other von Willebrand diseaseBillable
- D68.1Hereditary factor XI deficiencyBillable
- D68.2Hereditary deficiency of other clotting factorsBillable
- D68.3Hemorrhagic disorder due to circulating anticoagulantsHeader
- D68.31Hemorrhagic disorder due to intrns circ anticoag,antib,inhibHeader
- D68.311Acquired hemophiliaBillable
- D68.312Antiphospholipid antibody with hemorrhagic disorderBillable
- D68.318Other hemorrhagic disord due to intrns circ anticoag,antib,inhibBillable
- D68.32Hemorrhagic disord due to extrinsic circulating anticoagulantsBillable
- D68.4Acquired coagulation factor deficiencyBillable
- D68.5Primary thrombophiliaHeader
- D68.51Activated protein C resistanceBillable
- D68.52Prothrombin gene mutationBillable
- D68.59Other primary thrombophiliaBillable
- D68.6Other thrombophiliaHeader
- D68.61Antiphospholipid syndromeBillable
- D68.62Lupus anticoagulant syndromeBillable
- D68.69Other thrombophiliaBillable
- D68.8Other specified coagulation defectsBillable
- D68.9Coagulation defect, unspecifiedBillable
- D69Purpura and other hemorrhagic conditionsHeader
- D69.0Allergic purpuraBillable
- D69.1Qualitative platelet defectsHeader
- D69.11Glanzmann thrombastheniaBillable
- D69.19Other qualitative platelet defectsBillable
- D69.2Other nonthrombocytopenic purpuraBillable
- D69.3Immune thrombocytopenic purpuraBillable
- D69.4Other primary thrombocytopeniaHeader
- D69.41Evans syndromeBillable
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