| ICD-10-CM-2023 > D50-D89 > D80-D89 > D80 |
D80-D89 | Certain disorders involving the immune mechanism | |
Incl.: | defects in the complement system immunodeficiency disorders, except human immunodeficiency virus [HIV] disease sarcoidosis | |
Excl1.: | autoimmune disease (systemic) NOS (M35.9) functional disorders of polymorphonuclear neutrophils (D71) human immunodeficiency virus [HIV] disease (B20) | |
D80 | Immunodeficiency with predominantly antibody defects | |
D80.0 | Hereditary hypogammaglobulinemia | |
Info: | Autosomal recessive agammaglobulinemia (Swiss type) X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency) | |
D80.1 | Nonfamilial hypogammaglobulinemia | |
Info: | Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinemia [CVAgamma] Hypogammaglobulinemia NOS | |
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] | |
D80.6 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia | |
D80.7 | Transient hypogammaglobulinemia of infancy | |
D80.8 | Other immunodeficiencies with predominantly antibody defects | |
Info: | Kappa light chain deficiency | |
D80.9 | Immunodeficiency with predominantly antibody defects, unspecified | |
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