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 |
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 |
D8984 | IgG4-related disease |
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 |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 29 Mar 2024 17:03:46 CMS, code-revision=361, description-revision=1397 |