ICD-10-CM/PCS MS-DRG v42.0 Definitions Manual |
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MDC 16 Diseases and disorders of blood, blood forming organs and immunologic disorders |
Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders |
MCC | CC | DRG |
---|---|---|
Yes | n/a | 808 |
No | Yes | 809 |
No | No | 810 |
DRG 808 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC
DRG 809 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC
DRG 810 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC
PRINCIPAL DIAGNOSIS
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6103 | Fanconi anemia |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D700 | Congenital agranulocytosis |
D701 | Agranulocytosis secondary to cancer chemotherapy |
D702 | Other drug-induced agranulocytosis |
D703 | Neutropenia due to infection |
D704 | Cyclic neutropenia |
D708 | Other neutropenia |
D709 | Neutropenia, unspecified |
D71 | Functional disorders of polymorphonuclear neutrophils |
D720 | Genetic anomalies of leukocytes |
D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
D808 | Other immunodeficiencies with predominantly antibody defects |
D809 | Immunodeficiency with predominantly antibody defects, unspecified |
D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
D814 | Nezelof's syndrome |
D816 | Major histocompatibility complex class I deficiency |
D817 | Major histocompatibility complex class II deficiency |
D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
D8189 | Other combined immunodeficiencies |
D819 | Combined immunodeficiency, unspecified |
D820 | Wiskott-Aldrich syndrome |
D821 | Di George's syndrome |
D89810 | Acute graft-versus-host disease |
D89811 | Chronic graft-versus-host disease |
D89812 | Acute on chronic graft-versus-host disease |
D89813 | Graft-versus-host disease, unspecified |
T8600 | Unspecified complication of bone marrow transplant |
T8601 | Bone marrow transplant rejection |
T8602 | Bone marrow transplant failure |
T8603 | Bone marrow transplant infection |
T8609 | Other complications of bone marrow transplant |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 29 Mar 2024 17:03:46 CMS, code-revision=361, description-revision=1397 |