ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual
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DRAFT
ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual |
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| MDC 16 Diseases and disorders of blood, blood forming organs and immunologic disorders |
| Reticuloendothelial and immunity disorders |
| MCC | CC | DRG |
|---|---|---|
| Yes | n/a | 814 |
| No | Yes | 815 |
| No | No | 816 |
DRG 814 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC
DRG 815 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC
DRG 816 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC
PRINCIPAL DIAGNOSIS
| A182 | Tuberculous peripheral lymphadenopathy |
| A1885 | Tuberculosis of spleen |
| A281 | Cat-scratch disease |
| D150 | Benign neoplasm of thymus |
| D181 | Lymphangioma, any site |
| D360 | Benign neoplasm of lymph nodes |
| D3A091 | Benign carcinoid tumor of the thymus |
| D472 | Monoclonal gammopathy |
| D473 | Essential (hemorrhagic) thrombocythemia |
| D474 | Osteomyelofibrosis |
| D68312 | Antiphospholipid antibody with hemorrhagic disorder |
| D6851 | Activated protein C resistance |
| D6852 | Prothrombin gene mutation |
| D6859 | Other primary thrombophilia |
| D6861 | Antiphospholipid syndrome |
| D6862 | Lupus anticoagulant syndrome |
| D6869 | Other thrombophilia |
| D7210 | Eosinophilia, unspecified |
| D72110 | Idiopathic hypereosinophilic syndrome [IHES] |
| D72111 | Lymphocytic Variant Hypereosinophilic Syndrome [LHES] |
| D72118 | Other hypereosinophilic syndrome |
| D72119 | Hypereosinophilic syndrome [HES], unspecified |
| D7212 | Drug rash with eosinophilia and systemic symptoms syndrome |
| D7218 | Eosinophilia in diseases classified elsewhere |
| D7219 | Other eosinophilia |
| D72810 | Lymphocytopenia |
| D72818 | Other decreased white blood cell count |
| D72819 | Decreased white blood cell count, unspecified |
| D72820 | Lymphocytosis (symptomatic) |
| D72821 | Monocytosis (symptomatic) |
| D72822 | Plasmacytosis |
| D72823 | Leukemoid reaction |
| D72824 | Basophilia |
| D72825 | Bandemia |
| D72828 | Other elevated white blood cell count |
| D72829 | Elevated white blood cell count, unspecified |
| D7289 | Other specified disorders of white blood cells |
| D729 | Disorder of white blood cells, unspecified |
| D730 | Hyposplenism |
| D731 | Hypersplenism |
| D732 | Chronic congestive splenomegaly |
| D733 | Abscess of spleen |
| D734 | Cyst of spleen |
| D735 | Infarction of spleen |
| D7381 | Neutropenic splenomegaly |
| D7389 | Other diseases of spleen |
| D739 | Disease of spleen, unspecified |
| D750 | Familial erythrocytosis |
| D751 | Secondary polycythemia |
| D75838 | Other thrombocytosis |
| D75839 | Thrombocytosis, unspecified |
| D7589 | Other specified diseases of blood and blood-forming organs |
| D759 | Disease of blood and blood-forming organs, unspecified |
| D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
| D761 | Hemophagocytic lymphohistiocytosis |
| D762 | Hemophagocytic syndrome, infection-associated |
| D763 | Other histiocytosis syndromes |
| D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
| D800 | Hereditary hypogammaglobulinemia |
| D801 | Nonfamilial hypogammaglobulinemia |
| D802 | Selective deficiency of immunoglobulin A [IgA] |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D807 | Transient hypogammaglobulinemia of infancy |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D8481 | Immunodeficiency due to conditions classified elsewhere |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D890 | Polyclonal hypergammaglobulinemia |
| D892 | Hypergammaglobulinemia, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8944 | Hereditary alpha tryptasemia |
| D8949 | Other mast cell activation disorder |
| D89831 | Cytokine release syndrome, grade 1 |
| D89832 | Cytokine release syndrome, grade 2 |
| D89833 | Cytokine release syndrome, grade 3 |
| D89834 | Cytokine release syndrome, grade 4 |
| D89835 | Cytokine release syndrome, grade 5 |
| D89839 | Cytokine release syndrome, grade unspecified |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| E320 | Persistent hyperplasia of thymus |
| E321 | Abscess of thymus |
| E328 | Other diseases of thymus |
| E329 | Disease of thymus, unspecified |
| I881 | Chronic lymphadenitis, except mesenteric |
| I888 | Other nonspecific lymphadenitis |
| I889 | Nonspecific lymphadenitis, unspecified |
| I898 | Other specified noninfective disorders of lymphatic vessels and lymph nodes |
| I899 | Noninfective disorder of lymphatic vessels and lymph nodes, unspecified |
| L040 | Acute lymphadenitis of face, head and neck |
| L041 | Acute lymphadenitis of trunk |
| L042 | Acute lymphadenitis of upper limb |
| L043 | Acute lymphadenitis of lower limb |
| L048 | Acute lymphadenitis of other sites |
| L049 | Acute lymphadenitis, unspecified |
| Q8901 | Asplenia (congenital) |
| Q8909 | Congenital malformations of spleen |
| R161 | Splenomegaly, not elsewhere classified |
| R590 | Localized enlarged lymph nodes |
| R591 | Generalized enlarged lymph nodes |
| R599 | Enlarged lymph nodes, unspecified |
| R75 | Inconclusive laboratory evidence of human immunodeficiency virus [HIV] |
| R760 | Raised antibody titer |
| R768 | Other specified abnormal immunological findings in serum |
| R769 | Abnormal immunological finding in serum, unspecified |
| S3600XA | Unspecified injury of spleen, initial encounter |
| S36020A | Minor contusion of spleen, initial encounter |
| S36021A | Major contusion of spleen, initial encounter |
| S36029A | Unspecified contusion of spleen, initial encounter |
| S36030A | Superficial (capsular) laceration of spleen, initial encounter |
| S36031A | Moderate laceration of spleen, initial encounter |
| S36032A | Major laceration of spleen, initial encounter |
| S36039A | Unspecified laceration of spleen, initial encounter |
| S3609XA | Other injury of spleen, initial encounter |
| T8082XA | Complication of immune effector cellular therapy, initial encounter |
| Z9481 | Bone marrow transplant status |
| Z9484 | Stem cells transplant status |
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Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 16 Mar 2022 17:08:13 CMS, code-revision=333, description-revision=1331 |