 D80 |
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Immunodeficiency with predominantly antibody defects |
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 D80.0 |
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Hereditary hypogammaglobulinemia |
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| Autosomal recessive agammaglobulinemia (Swiss type) | | X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency) |
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| D80.1 |
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Nonfamilial hypogammaglobulinemia |
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| Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes | | Common variable agammaglobulinemia [CVAgamma] | | Hypogammaglobulinemia NOS |
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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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| D80.7 |
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Transient hypogammaglobulinemia of infancy |
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| D80.8 |
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Other immunodeficiencies with predominantly antibody defects |
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| Kappa light chain deficiency |
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| D80.9 |
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Immunodeficiency with predominantly antibody defects, unspecified |
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