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 recessive agammaglobulinemia (Swiss type)
 * X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
 * D80.1 Nonfamilial hypogammaglobulinemia
 * 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
 * Kappa light chain deficiency
 * D80.9 Immunodeficiency with predominantly antibody defects, unspecified

D81 Combined immunodeficiencies

 * Excludes1: autosomal recessive agammaglobulinemia (Swiss type) (D80.0)
 * D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
 * D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
 * D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
 * D81.3 Adenosine deaminase [ADA] deficiency
 * D81.4 Nezelof's syndrome
 * D81.5 Purine nucleoside phosphorylase [PNP] deficiency
 * D81.6 Major histocompatibility complex class I deficiency
 * Bare lymphocyte syndrome
 * D81.7 Major histocompatibility complex class II deficiency
 * D81.8 Other combined immunodeficiencies
 * D81.81 Biotin-dependent carboxylase deficiency
 * Multiple carboxylase deficiency
 * Excludes1: biotin-dependent carboxylase deficiency due to dietary deficiency of biotin (E53.8)
 * D81.810 Biotinidase deficiency
 * D81.818 Other biotin-dependent carboxylase deficiency
 * Holocarboxylase synthetase deficiency
 * Other multiple carboxylase deficiency
 * D81.819 Biotin-dependent carboxylase deficiency, unspecified
 * Multiple carboxylase deficiency, unspecified
 * D81.