CC Codes: Diseases of the Blood and Blood-Forming Organs (D50-D89)
110 codes in D50-D89 are a CC as a secondary diagnosis under MS-DRG v44.0 (FY2027). Full CC list
D55-D59
| D58.8 | Other specified hereditary hemolytic anemias |
| D58.9 | Hereditary hemolytic anemia, unspecified |
| D59.0 | Drug-induced autoimmune hemolytic anemia |
| D59.10 | Autoimmune hemolytic anemia, unspecified |
| D59.11 | Warm autoimmune hemolytic anemia |
| D59.12 | Cold autoimmune hemolytic anemia |
| D59.13 | Mixed type autoimmune hemolytic anemia |
| D59.19 | Other autoimmune hemolytic anemia |
| D59.2 | Drug-induced nonautoimmune hemolytic anemia |
| D59.4 | Other nonautoimmune hemolytic anemias |
| D59.9 | Acquired hemolytic anemia, unspecified |
D60-D64
| D61.01 | Constitutional (pure) red blood cell aplasia |
| D61.02 | Shwachman-Diamond syndrome |
| D61.03 | Fanconi anemia |
| D61.09 | Other constitutional aplastic anemia |
| D61.818 | Other pancytopenia |
| D61.82 | Myelophthisis |
| D61.9 | Aplastic anemia, unspecified |
| D62 | Acute posthemorrhagic anemia |
D65-D69
| D68.00 | Von Willebrand disease, unspecified |
| D68.01 | Von Willebrand disease, type 1 |
| D68.020 | Von Willebrand disease, type 2A |
| D68.021 | Von Willebrand disease, type 2B |
| D68.022 | Von Willebrand disease, type 2M |
| D68.023 | Von Willebrand disease, type 2N |
| D68.029 | Von Willebrand disease, type 2, unspecified |
| D68.03 | Von Willebrand disease, type 3 |
| D68.04 | Acquired von Willebrand disease |
| D68.09 | Other von Willebrand disease |
| D68.1 | Hereditary factor XI deficiency |
| D68.2 | Hereditary deficiency of other clotting factors |
| D68.311 | Acquired hemophilia |
| D68.312 | Antiphospholipid antibody with hemorrhagic disorder |
| D68.318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
| D68.32 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
| D68.4 | Acquired coagulation factor deficiency |
| D68.51 | Activated protein C resistance |
| D68.52 | Prothrombin gene mutation |
| D68.59 | Other primary thrombophilia |
| D68.61 | Antiphospholipid syndrome |
| D68.62 | Lupus anticoagulant syndrome |
| D68.69 | Other thrombophilia |
| D68.8 | Other specified coagulation defects |
| D68.9 | Coagulation defect, unspecified |
| D69.0 | Allergic purpura |
| D69.3 | Immune thrombocytopenic purpura |
| D69.41 | Evans syndrome |
| D69.42 | Congenital and hereditary thrombocytopenia purpura |
D70-D77
| D74.0 | Congenital methemoglobinemia |
| D74.8 | Other methemoglobinemias |
| D74.9 | Methemoglobinemia, unspecified |
| D75.81 | Myelofibrosis |
| D76.1 | Hemophagocytic lymphohistiocytosis |
| D76.2 | Hemophagocytic syndrome, infection-associated |
| D76.3 | Other histiocytosis syndromes |
D78
| D78.01 | Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen |
| D78.02 | Intraoperative hemorrhage and hematoma of the spleen complicating other procedure |
| D78.11 | Accidental puncture and laceration of the spleen during a procedure on the spleen |
| D78.12 | Accidental puncture and laceration of the spleen during other procedure |
| D78.21 | Postprocedural hemorrhage of the spleen following a procedure on the spleen |
| D78.22 | Postprocedural hemorrhage of the spleen following other procedure |
| D78.31 | Postprocedural hematoma of the spleen following a procedure on the spleen |
| D78.32 | Postprocedural hematoma of the spleen following other procedure |
| D78.33 | Postprocedural seroma of the spleen following a procedure on the spleen |
| D78.34 | Postprocedural seroma of the spleen following other procedure |
| D78.81 | Other intraoperative complications of the spleen |
| D78.89 | Other postprocedural complications of the spleen |
D80-D89
| D80.0 | Hereditary hypogammaglobulinemia |
| D80.1 | Nonfamilial hypogammaglobulinemia |
| D80.2 | Selective deficiency of immunoglobulin A [IgA] |
| D80.3 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D80.4 | Selective deficiency of immunoglobulin M [IgM] |
| D80.5 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D80.6 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D80.7 | Transient hypogammaglobulinemia of infancy |
| D80.8 | Other immunodeficiencies with predominantly antibody defects |
| D80.9 | Immunodeficiency with predominantly antibody defects, unspecified |
| D81.0 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D81.1 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D81.2 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D81.30 | Adenosine deaminase deficiency, unspecified |
| D81.31 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
| D81.32 | Adenosine deaminase 2 deficiency |
| D81.39 | Other adenosine deaminase deficiency |
| D81.4 | Nezelof's syndrome |
| D81.5 | Purine nucleoside phosphorylase [PNP] deficiency |
| D81.6 | Major histocompatibility complex class I deficiency |
| D81.7 | Major histocompatibility complex class II deficiency |
| D81.82 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D81.89 | Other combined immunodeficiencies |
| D81.9 | Combined immunodeficiency, unspecified |
| D82.0 | Wiskott-Aldrich syndrome |
| D82.1 | Di George's syndrome |
| D83.0 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D83.1 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D83.2 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D83.8 | Other common variable immunodeficiencies |
| D83.9 | Common variable immunodeficiency, unspecified |
| D84.81 | Immunodeficiency due to conditions classified elsewhere |
| D84.821 | Immunodeficiency due to drugs |
| D84.822 | Immunodeficiency due to external causes |
| D84.89 | Other immunodeficiencies |
| D84.9 | Immunodeficiency, unspecified |
| D89.810 | Acute graft-versus-host disease |
| D89.811 | Chronic graft-versus-host disease |
| D89.812 | Acute on chronic graft-versus-host disease |
| D89.813 | Graft-versus-host disease, unspecified |
| D89.833 | Cytokine release syndrome, grade 3 |
| D89.834 | Cytokine release syndrome, grade 4 |
| D89.835 | Cytokine release syndrome, grade 5 |