Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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D80–D89 Certain disorders involving the immune mechanism |
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D80 |
Immunodeficiency with predominantly antibody defects |
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D80.0 |
Hereditary hypogammaglobulinaemia Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia (Bruton) (with growth hormone deficiency) |
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D80.1 |
Nonfamilial hypogammaglobulinaemia Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia (CVAgamma) Hypogammaglobulinaemia NOS |
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D80.2 |
Selective deficiency of immunoglobulin A (IgA) |
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D80.3 |
Selective deficiency of immunoglobulin G (IgG) subclasses |
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D80.4 |
Selective deficiency of immunoglobulin M (IgM) |
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D80.5 |
Immunodeficiency with increased immunoglobulin M (IgM) |
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D80.6 |
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia |
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D80.7 |
Transient hypogammaglobulinaemia of infancy |
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D80.8 |
Other immunodeficiencies with predominantly antibody defects Kappa light chain deficiency |
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D80.9 |
Immunodeficiency with predominantly antibody defects, unspecified |
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D81 |
Combined immunodeficiencies |
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D81.0 |
Severe combined immunodeficiency (SCID) with reticular dysgenesis |
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D81.1 |
Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers |
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D81.2 |
Severe combined immunodeficiency (SCID) with low or normal B-cell numbers |
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D81.3 |
Adenosine deaminase deficiency (ADA) |
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D81.4 |
Nezelof's syndrome |
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D81.5 |
Purine nucleoside phosphorylase deficiency (PNP) |
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D81.6 |
Major histocompatibility complex class I deficiency Bare lymphocyte syndrome |
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D81.7 |
Major histocompatibility complex class II deficiency |
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D81.8 |
Other combined immunodeficiencies Biotin-dependent carboxylase deficiency |
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D81.9 |
Combined immunodeficiency, unspecified Severe combined immunodeficiency disorder (SCID) NOS |
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D82 |
Immunodeficiency associated with other major defects |
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D82.0 |
Wiskott-Aldrich syndrome Immunodeficiency with thrombocytopenia and eczema |
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D82.1 |
Di George's syndrome |
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D82.2 |
Immunodeficiency with short-limbed stature |
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D82.3 |
Immunodeficiency following hereditary defective response to Epstein-Barr virus X-linked lymphoproliferative disease |
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D82.4 |
Hyperimmunoglobulin E syndrome (IgE) |
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D83 |
Common variable immunodeficiency |
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D84 |
Other 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 C1 esterase inhibitor deficiency (C1-INH) |
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D84.8 |
Other specified immunodeficiencies |
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D84.9 |
Immunodeficiency, unspecified |
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D86 |
Sarcoidosis |
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D86.0 |
Sarcoidosis of lung |
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D86.1 |
Sarcoidosis of lymph nodes |
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D86.2 |
Sarcoidosis of lung with sarcoidosis of lymph nodes |
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D86.3 |
Sarcoidosis of skin |
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D86.8 |
Sarcoidosis of other and combined sites |
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D89 |
Other disorders involving the immune mechanism, not elsewhere classified |
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D89.0 |
Polyclonal hypergammaglobulinaemia Benign hypergammaglobulinaemic purpura Polyclonal gammopathy NOS |
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D89.1 |
Cryoglobulinaemia |
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D89.2 |
Hypergammaglobulinaemia, unspecified |
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D89.8 |
Other specified disorders involving the immune mechanism, not elsewhere classified |
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D89.9 |
Disorder involving the immune mechanism, unspecified |
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D80.8 |
Other immunodeficiencies with predominantly antibody defects Kappa light chain deficiency |
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D80.9 |
Immunodeficiency with predominantly antibody defects, unspecified |
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D81 |
Combined immunodeficiencies |
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D81.0 |
Severe combined immunodeficiency (SCID) with reticular dysgenesis |
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D81.1 |
Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers |
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D81.2 |
Severe combined immunodeficiency (SCID) with low or normal B-cell numbers |
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D81.3 |
Adenosine deaminase deficiency (ADA) |
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D81.4 |
Nezelof's syndrome |
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D81.5 |
Purine nucleoside phosphorylase deficiency (PNP) |
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D81.6 |
Major histocompatibility complex class I deficiency Bare lymphocyte syndrome |
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D81.7 |
Major histocompatibility complex class II deficiency |
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D81.8 |
Other combined immunodeficiencies Biotin-dependent carboxylase deficiency |
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D81.9 |
Combined immunodeficiency, unspecified Severe combined immunodeficiency disorder (SCID) NOS |
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D82 |
Immunodeficiency associated with other major defects |
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D82.0 |
Wiskott-Aldrich syndrome Immunodeficiency with thrombocytopenia and eczema |
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D82.1 |
Di George's syndrome |
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D82.2 |
Immunodeficiency with short-limbed stature |
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D82.3 |
Immunodeficiency following hereditary defective response to Epstein-Barr virus X-linked lymphoproliferative disease |
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D82.4 |
Hyperimmunoglobulin E syndrome (IgE) |
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D83 |
Common variable immunodeficiency |
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D84 |
Other 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 C1 esterase inhibitor deficiency (C1-INH) |
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D84.8 |
Other specified immunodeficiencies |
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D84.9 |
Immunodeficiency, unspecified |
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D86 |
Sarcoidosis |
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D86.0 |
Sarcoidosis of lung |
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D86.1 |
Sarcoidosis of lymph nodes |
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D86.2 |
Sarcoidosis of lung with sarcoidosis of lymph nodes |
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D86.3 |
Sarcoidosis of skin |
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D86.8 |
Sarcoidosis of other and combined sites |
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D89 |
Other disorders involving the immune mechanism, not elsewhere classified |
|
D89.0 |
Polyclonal hypergammaglobulinaemia Benign hypergammaglobulinaemic purpura Polyclonal gammopathy NOS |
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D89.1 |
Cryoglobulinaemia |
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D89.2 |
Hypergammaglobulinaemia, unspecified |
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D89.8 |
Other specified disorders involving the immune mechanism, not elsewhere classified |
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D89.9 |
Disorder involving the immune mechanism, unspecified |
