23,524 codes
Non-billable / header codes
Category and subcategory headers that need more characters before they can be reported. Source: ICD-10-CM FY2027.
Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- D50Iron deficiency anemia
- D51Vitamin B12 deficiency anemia
- D52Folate deficiency anemia
- D53Other nutritional anemias
- D55Anemia due to enzyme disorders
- D55.2Anemia due to disorders of glycolytic enzymes
- D56Thalassemia
- D57Sickle-cell disorders
- D57.0Hb-SS disease with crisis
- D57.2Sickle-cell/Hb-C disease
- D57.21Sickle-cell/Hb-C disease with crisis
- D57.4Sickle-cell thalassemia
- D57.41Sickle-cell thalassemia, unspecified, with crisis
- D57.43Sickle-cell thalassemia beta zero with crisis
- D57.45Sickle-cell thalassemia beta plus with crisis
- D57.8Other sickle-cell disorders
- D57.81Other sickle-cell disorders with crisis
- D58Other hereditary hemolytic anemias
- D59Acquired hemolytic anemia
- D59.1Other autoimmune hemolytic anemias
- D59.3Hemolytic-uremic syndrome
- D60Acquired pure red cell aplasia [erythroblastopenia]
- D61Other aplastic anemias and other bone marrow failure syndromes
- D61.0Constitutional aplastic anemia
- D61.8Other specified aplastic anemias and other bone marrow failure syndromes
- D61.81Pancytopenia
- D63Anemia in chronic diseases classified elsewhere
- D64Other anemias
- D64.8Other specified anemias
- D68Other coagulation defects
- D68.0Von Willebrand disease
- D68.02Von Willebrand disease, type 2
- D68.3Hemorrhagic disorder due to circulating anticoagulants
- D68.31Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
- D68.5Primary thrombophilia
- D68.6Other thrombophilia
- D69Purpura and other hemorrhagic conditions
- D69.1Qualitative platelet defects
- D69.4Other primary thrombocytopenia
- D69.5Secondary thrombocytopenia
- D70Neutropenia
- D71Functional disorders of polymorphonuclear neutrophils
- D72Other disorders of white blood cells
- D72.1Eosinophilia
- D72.11Hypereosinophilic syndrome [HES]
- D72.8Other specified disorders of white blood cells
- D72.81Decreased white blood cell count
- D72.82Elevated white blood cell count
- D73Diseases of spleen
- D73.8Other diseases of spleen
- D74Methemoglobinemia
- D75Other and unspecified diseases of blood and blood-forming organs
- D75.8Other specified diseases of blood and blood-forming organs
- D75.82Heparin induced thrombocytopenia (HIT)
- D75.83Thrombocytosis
- D76Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue
- D78Intraoperative and postprocedural complications of the spleen
- D78.0Intraoperative hemorrhage and hematoma of the spleen complicating a procedure
- D78.1Accidental puncture and laceration of the spleen during a procedure
- D78.2Postprocedural hemorrhage of the spleen following a procedure
- D78.3Postprocedural hematoma and seroma of the spleen following a procedure
- D78.8Other intraoperative and postprocedural complications of the spleen
- D80Immunodeficiency with predominantly antibody defects
- D81Combined immunodeficiencies
- D81.3Adenosine deaminase [ADA] deficiency
- D81.8Other combined immunodeficiencies
- D81.81Biotin-dependent carboxylase deficiency
- D82Immunodeficiency associated with other major defects
- D83Common variable immunodeficiency
- D84Other immunodeficiencies
- D84.8Other specified immunodeficiencies
- D84.82Immunodeficiency due to drugs and external causes
- D86Sarcoidosis
- D86.8Sarcoidosis of other sites
- D89Other disorders involving the immune mechanism, not elsewhere classified
- D89.4Mast cell activation syndrome and related disorders
- D89.8Other specified disorders involving the immune mechanism, not elsewhere classified
- D89.81Graft-versus-host disease
- D89.83Cytokine release syndrome