ICD-10-CM 2027 · D80-D89
Certain disorders involving the immune mechanism
Part of chapter 3, diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
About D80-D89
D80Immunodeficiency with predominantly antibody defects
- D80.0Hereditary hypogammaglobulinemia
- D80.1Nonfamilial hypogammaglobulinemia
- D80.2Selective deficiency of immunoglobulin A [IgA]
- D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
- D80.4Selective deficiency of immunoglobulin M [IgM]
- D80.5Immunodeficiency with increased immunoglobulin M [IgM]
- D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
- D80.7Transient hypogammaglobulinemia of infancy
- D80.8Other immunodeficiencies with predominantly antibody defects
- D80.9Immunodeficiency with predominantly antibody defects, unspecified
D81Combined immunodeficiencies
- D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
- D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
- D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
- D81.3Adenosine deaminase [ADA] deficiency
- D81.4Nezelof's syndrome
- D81.5Purine nucleoside phosphorylase [PNP] deficiency
- D81.6Major histocompatibility complex class I deficiency
- D81.7Major histocompatibility complex class II deficiency
- D81.8Other combined immunodeficiencies
- D81.9Combined immunodeficiency, unspecified
D82Immunodeficiency associated with other major defects
- D82.0Wiskott-Aldrich syndrome
- D82.1Di George's syndrome
- D82.2Immunodeficiency with short-limbed stature
- D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
- D82.4Hyperimmunoglobulin E [IgE] syndrome
- D82.8Immunodeficiency associated with other specified major defects
- D82.9Immunodeficiency associated with major defect, unspecified
D83Common variable immunodeficiency
- D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
- D83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
- D83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
- D83.8Other common variable immunodeficiencies
- D83.9Common variable immunodeficiency, unspecified
D84Other immunodeficiencies
D86Sarcoidosis
D89Other disorders involving the immune mechanism, not elsewhere classified
- D89.0Polyclonal hypergammaglobulinemia
- D89.1Cryoglobulinemia
- D89.2Hypergammaglobulinemia, unspecified
- D89.3Immune reconstitution syndrome
- D89.4Mast cell activation syndrome and related disorders
- D89.8Other specified disorders involving the immune mechanism, not elsewhere classified
- D89.9Disorder involving the immune mechanism, unspecified