It is the provider’s responsibility to select codes carried out to the highest level of specificity and selected from the ICD-10-CM code book appropriate to the year in which the service is rendered for the claim(s) submitted.
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B20
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Human immunodeficiency virus [HIV] disease |
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D80.0
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Hereditary hypogammaglobulinemia |
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D80.1
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Nonfamilial hypogammaglobulinemia |
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D80.2
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Selective deficiency of immunoglobulin A [IgA] |
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D80.3
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Selective deficiency of immunoglobulin G [IgG] subclasses |
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D80.4
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Selective deficiency of immunoglobulin M [IgM] |
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D80.5
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Immunodeficiency with increased immunoglobulin M [IgM] |
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D80.6
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Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
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D80.8
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Other immunodeficiencies with predominantly antibody defects |
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D81.0
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Severe combined immunodeficiency [SCID] with reticular dysgenesis |
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D81.1
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Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
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D81.2
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Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
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D81.31
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Severe combined immunodeficiency due to adenosine deaminase deficiency |
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D81.4
|
Nezelof's syndrome |
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D81.5
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Purine nucleoside phosphorylase [PNP] deficiency |
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D81.6
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Major histocompatibility complex class I deficiency |
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D81.7
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Major histocompatibility complex class II deficiency |
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D81.810
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Biotinidase deficiency |
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D81.818
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Other biotin-dependent carboxylase deficiency |
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D81.89
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Other combined immunodeficiencies |
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D82.0
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Wiskott-Aldrich syndrome |
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D82.1
|
Di George's syndrome |
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D82.2
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Immunodeficiency with short-limbed stature |
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D82.3
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Immunodeficiency following hereditary defective response to Epstein-Barr virus |
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D82.4
|
Hyperimmunoglobulin E [IgE] syndrome |
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D82.8
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Immunodeficiency associated with other specified major defects |
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D83.0
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Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
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D83.1
|
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
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D83.2
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Common variable immunodeficiency with autoantibodies to B- or T-cells |
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D83.8
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Other common variable immunodeficiencies |
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D84.0
|
Lymphocyte function antigen-1 [LFA-1] defect |
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D84.1
|
Defects in the complement system |
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D84.81
|
Immunodeficiency due to conditions classified elsewhere |
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D84.821
|
Immunodeficiency due to drugs |
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D84.822
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Immunodeficiency due to external causes |
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D84.89
|
Other immunodeficiencies |
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D89.0
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Polyclonal hypergammaglobulinemia |
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D89.1
|
Cryoglobulinemia |
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D89.3
|
Immune reconstitution syndrome |
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D89.41
|
Monoclonal mast cell activation syndrome |
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D89.42
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Idiopathic mast cell activation syndrome |
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D89.43
|
Secondary mast cell activation |
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D89.49
|
Other mast cell activation disorder |
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D89.810
|
Acute graft-versus-host disease |
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D89.811
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Chronic graft-versus-host disease |
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D89.812
|
Acute on chronic graft-versus-host disease |
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D89.82
|
Autoimmune lymphoproliferative syndrome [ALPS] |
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D89.89
|
Other specified disorders involving the immune mechanism, not elsewhere classified |
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Z94.0
|
Kidney transplant status |
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Z94.1
|
Heart transplant status |
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Z94.2
|
Lung transplant status |
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Z94.3
|
Heart and lungs transplant status |
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Z94.4
|
Liver transplant status |
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Z94.5
|
Skin transplant status |
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Z94.6
|
Bone transplant status |
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Z94.81
|
Bone marrow transplant status |
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Z94.82
|
Intestine transplant status |
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Z94.83
|
Pancreas transplant status |
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Z94.84
|
Stem cells transplant status |