MS-DRG 816

Principal Diagnosis - Pdx

• 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
• D72.10 Eosinophilia, unspecified
• D72.110 Idiopathic hypereosinophilic syndrome [IHES]
• D72.111 Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
• D72.118 Other hypereosinophilic syndrome
• D72.119 Hypereosinophilic syndrome [HES], unspecified
• D72.12 Drug rash with eosinophilia and systemic symptoms syndrome
• D72.18 Eosinophilia in diseases classified elsewhere
• D72.19 Other 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
• D75.838 Other thrombocytosis
• D75.839 Thrombocytosis, unspecified
• 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
• D84.81 Immunodeficiency due to conditions classified elsewhere
• D84.821 Immunodeficiency due to drugs
• D84.822 Immunodeficiency due to external causes
• D84.89 Other 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
• D89.44 Hereditary alpha tryptasemia
• D89.49 Other mast cell activation disorder
• D89.831 Cytokine release syndrome, grade 1
• D89.832 Cytokine release syndrome, grade 2
• D89.833 Cytokine release syndrome, grade 3
• D89.834 Cytokine release syndrome, grade 4
• D89.835 Cytokine release syndrome, grade 5
• D89.839 Cytokine release syndrome, grade unspecified
• D89.84 IgG4-related disease
• 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