15,083 codes
CC codes (complication or comorbidity)
Secondary diagnoses that raise an inpatient stay to the middle-severity MS-DRG in a family, unless excluded for the principal diagnosis. Source: MS-DRG v44 Definitions Manual, Appendix C.
Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- D58.8Other specified hereditary hemolytic anemias
- D58.9Hereditary hemolytic anemia, unspecified
- D59.0Drug-induced autoimmune hemolytic anemia
- D59.10Autoimmune hemolytic anemia, unspecified
- D59.11Warm autoimmune hemolytic anemia
- D59.12Cold autoimmune hemolytic anemia
- D59.13Mixed type autoimmune hemolytic anemia
- D59.19Other autoimmune hemolytic anemia
- D59.2Drug-induced nonautoimmune hemolytic anemia
- D59.4Other nonautoimmune hemolytic anemias
- D59.9Acquired hemolytic anemia, unspecified
- D61.01Constitutional (pure) red blood cell aplasia
- D61.02Shwachman-Diamond syndrome
- D61.03Fanconi anemia
- D61.09Other constitutional aplastic anemia
- D61.818Other pancytopenia
- D61.82Myelophthisis
- D61.9Aplastic anemia, unspecified
- D62Acute posthemorrhagic anemia
- 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
- D68.61Antiphospholipid syndrome
- D68.62Lupus anticoagulant syndrome
- D68.69Other thrombophilia
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D69.0Allergic purpura
- D69.3Immune thrombocytopenic purpura
- D69.41Evans syndrome
- D69.42Congenital and hereditary thrombocytopenia purpura
- D74.0Congenital methemoglobinemia
- D74.8Other methemoglobinemias
- D74.9Methemoglobinemia, unspecified
- D75.81Myelofibrosis
- D76.1Hemophagocytic lymphohistiocytosis
- D76.2Hemophagocytic syndrome, infection-associated
- D76.3Other histiocytosis syndromes
- D78.01Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
- D78.02Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
- D78.11Accidental puncture and laceration of the spleen during a procedure on the spleen
- D78.12Accidental puncture and laceration of the spleen during other procedure
- D78.21Postprocedural hemorrhage of the spleen following a procedure on the spleen
- D78.22Postprocedural hemorrhage of the spleen following other procedure
- D78.31Postprocedural hematoma of the spleen following a procedure on the spleen
- D78.32Postprocedural hematoma of the spleen following other procedure
- D78.33Postprocedural seroma of the spleen following a procedure on the spleen
- D78.34Postprocedural seroma of the spleen following other procedure
- D78.81Other intraoperative complications of the spleen
- D78.89Other postprocedural complications of the spleen
- D80.0Hereditary hypogammaglobulinemia
- D80.1Nonfamilial hypogammaglobulinemia
- D80.2Selective deficiency of immunoglobulin A [IgA]
- D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
- D80.4Selective deficiency of immunoglobulin M [IgM]
- D80.5Immunodeficiency with increased immunoglobulin M [IgM]
- D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
- D80.7Transient hypogammaglobulinemia of infancy
- D80.8Other immunodeficiencies with predominantly antibody defects
- D80.9Immunodeficiency with predominantly antibody defects, unspecified
- D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
- D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
- D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
- D81.30Adenosine deaminase deficiency, unspecified
- D81.31Severe combined immunodeficiency due to adenosine deaminase deficiency
- D81.32Adenosine deaminase 2 deficiency
- D81.39Other adenosine deaminase deficiency
- D81.4Nezelof's syndrome
- D81.5Purine nucleoside phosphorylase [PNP] deficiency
- D81.6Major histocompatibility complex class I deficiency
- D81.7Major histocompatibility complex class II deficiency
- D81.82Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
- D81.89Other combined immunodeficiencies
- D81.9Combined immunodeficiency, unspecified
- D82.0Wiskott-Aldrich syndrome
- D82.1Di George's syndrome
- D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
- D83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
- D83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
- D83.8Other common variable immunodeficiencies
- D83.9Common variable immunodeficiency, unspecified
- D84.81Immunodeficiency due to conditions classified elsewhere
- D84.821Immunodeficiency due to drugs
- D84.822Immunodeficiency due to external causes
- D84.89Other immunodeficiencies
- D84.9Immunodeficiency, unspecified
- D89.810Acute graft-versus-host disease
- D89.811Chronic graft-versus-host disease
- D89.812Acute on chronic graft-versus-host disease
- D89.813Graft-versus-host disease, unspecified