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2. MS-DRG

DRG 814

Reticuloendothelial and immunity disorders with mcc

• 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
• D75.A Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
• D76.1 Hemophagocytic lymphohistiocytosis
• D76.2 Hemophagocytic syndrome, infection-associated
• D76.3 Other histiocytosis syndromes
• D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
• 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 Immunodeficiency following hereditary defective response to Epstein-Barr virus
• D82.4 Hyperimmunoglobulin E [IgE] syndrome
• D82.8 Immunodeficiency associated with other specified major defects
• D82.9 Immunodeficiency associated with major defect, unspecified
• D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
• D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
• D83.2 Common variable immunodeficiency with 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 Other specified disorders involving the immune mechanism, not elsewhere classified
• D89.9 Disorder involving the immune mechanism, unspecified
• E32.0 Persistent hyperplasia of thymus
• E32.1 Abscess 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 Other specified noninfective disorders of lymphatic vessels and lymph nodes
• I89.9 Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
• L04.0 Acute lymphadenitis of face, head and neck
• L04.1 Acute lymphadenitis of trunk
• L04.2 Acute lymphadenitis of upper limb
• L04.3 Acute lymphadenitis of lower limb
• L04.8 Acute lymphadenitis of other sites
• L04.9 Acute lymphadenitis, unspecified
• 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 immunodeficiency virus [HIV]
• R76.0 Raised antibody titer
• R76.8 Other specified abnormal immunological findings in serum
• R76.9 Abnormal immunological finding in serum, unspecified
• S36.00XA Unspecified injury of spleen, initial encounter
• S36.020A Minor contusion of spleen, initial encounter
• S36.021A Major contusion of spleen, initial encounter
• S36.029A Unspecified contusion of spleen, initial encounter
• S36.030A Superficial (capsular) laceration of spleen, initial encounter
• S36.031A Moderate laceration of spleen, initial encounter
• S36.032A Major laceration of spleen, initial encounter
• S36.039A Unspecified laceration of spleen, initial encounter
• S36.09XA Other injury of spleen, initial encounter
• Z94.81 Bone marrow transplant status
• Z94.84 Stem cells transplant status