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
  • 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