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
- D72.10 - 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
- 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
- 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
- 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
- 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