| ICD10 (CM) Code | Description |
| 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 dehydrgnse (G6PD) defic without anemia |
| 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 |
| D84.81
|
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
|
Oth disrd involving the immune mechanism, NEC |
| 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
|
Oth noninfective disorders of lymphatic vessels and nodes |
| I89.9
|
Noninfective disorder of lymphatic vessels and nodes, unsp |
| 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 immunodef virus |
| 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, init encntr |
| 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 |
| T80.82XA
|
Complication of immune effector cellular therapy, init |
| Z94.81
|
Bone marrow transplant status |
| Z94.84
|
Stem cells transplant status |
