DIAGNOSTIC RELATED GROUP MS-DRG V34.0 - RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC

    • A18.2 - Tuberculous peripheral lymphadenopathy
    • A18.85 - Tuberculosis of spleen
    • A28.1 - Cat-scratch disease
    • D15.0 - Benign neoplasm of thymus
    • D18.1 - Lymphangioma, any site
    • D36.0 - Benign neoplasm of lymph nodes
    • D3A.091 - Benign carcinoid tumor of the thymus
    • D47.2 - Monoclonal gammopathy
    • D47.3 - Essential (hemorrhagic) thrombocythemia
    • D47.4 - Osteomyelofibrosis
    • D68.312 - Antiphospholipid antibody with hemorrhagic disorder
    • 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
    • D72.1 - Eosinophilia
    • D72.810 - Lymphocytopenia
    • D72.818 - Other decreased white blood cell count
    • D72.819 - Decreased white blood cell count, unspecified
    • D72.820 - Lymphocytosis (symptomatic)
    • D72.821 - Monocytosis (symptomatic)
    • D72.822 - Plasmacytosis
    • D72.823 - Leukemoid reaction
    • D72.824 - Basophilia
    • D72.825 - Bandemia
    • D72.828 - Other elevated white blood cell count
    • D72.829 - Elevated white blood cell count, unspecified
    • D72.89 - Other specified disorders of white blood cells
    • D72.9 - Disorder of white blood cells, unspecified
    • D73.0 - Hyposplenism
    • D73.1 - Hypersplenism
    • D73.2 - Chronic congestive splenomegaly
    • D73.3 - Abscess of spleen
    • D73.4 - Cyst of spleen
    • D73.5 - Infarction of spleen
    • D73.81 - Neutropenic splenomegaly
    • D73.89 - Other diseases of spleen
    • D73.9 - Disease of spleen, unspecified
    • D75.0 - Familial erythrocytosis
    • D75.1 - Secondary polycythemia
    • D75.89 - Other specified diseases of blood and blood-forming organs
    • D75.9 - Disease of blood and blood-forming organs, unspecified
    • D76.1 - Hemophagocytic lymphohistiocytosis
    • D76.2 - Hemophagocytic syndrome, infection-associated
    • D76.3 - Other histiocytosis syndromes
    • D77 - Oth disord of bld/bld-frm organs in diseases classd elswhr
    • 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]
    • D80.7 - Transient hypogammaglobulinemia of infancy
    • D82.2 - Immunodeficiency with short-limbed stature
    • D82.3 - Immunodef fol heredit defctv response to Epstein-Barr virus
    • D82.4 - Hyperimmunoglobulin E [IgE] syndrome
    • D82.8 - Immunodeficiency associated with oth major defects
    • D82.9 - Immunodeficiency associated with major defect, unspecified
    • D83.0 - Com variab immunodef w predom abnlt of B-cell nums & functn
    • D83.1 - Com variab immunodef w predom immunoreg T-cell disorders
    • D83.2 - Common variable immunodef w autoantibodies to B- or T-cells
    • D83.8 - Other common variable immunodeficiencies
    • D83.9 - Common variable immunodeficiency, unspecified
    • D84.0 - Lymphocyte function antigen-1 [LFA-1] defect
    • D84.8 - Other specified immunodeficiencies
    • D84.9 - Immunodeficiency, unspecified
    • D89.0 - Polyclonal hypergammaglobulinemia
    • D89.2 - Hypergammaglobulinemia, unspecified
    • D89.3 - Immune reconstitution syndrome
    • D89.40 - Mast cell activation, unspecified
    • D89.41 - Monoclonal mast cell activation syndrome
    • D89.42 - Idiopathic mast cell activation syndrome
    • D89.43 - Secondary mast cell activation
    • D89.49 - Other mast cell activation disorder
    • D89.89 - Oth disrd involving the immune mechanism, NEC
    • D89.9 - Disorder involving the immune mechanism, unspecified
    • E32.0 - Persistent hyperplasia of thymus
    • E32.8 - Other diseases of thymus
    • E32.9 - Disease of thymus, unspecified
    • I88.1 - Chronic lymphadenitis, except mesenteric
    • I88.8 - Other nonspecific lymphadenitis
    • I88.9 - Nonspecific lymphadenitis, unspecified
    • I89.8 - Oth noninfective disorders of lymphatic vessels and nodes
    • I89.9 - Noninfective disorder of lymphatic vessels and nodes, unsp
    • Q89.01 - Asplenia (congenital)
    • Q89.09 - Congenital malformations of spleen
    • R16.1 - Splenomegaly, not elsewhere classified
    • R59.0 - Localized enlarged lymph nodes
    • R59.1 - Generalized enlarged lymph nodes
    • R59.9 - Enlarged lymph nodes, unspecified
    • R75 - Inconclusive laboratory evidence of human immunodef virus
    • R76.0 - Raised antibody titer
    • R76.8 - Other specified abnormal immunological findings in serum
    • R76.9 - Abnormal immunological finding in serum, unspecified
    • Z94.81 - Bone marrow transplant status
    • Z94.84 - Stem cells transplant status