D80 | Immunodeficiency with predominantly antibody defects |
D80.0 | Hereditary hypogammaglobulinemia |
D80.1 | Nonfamilial hypogammaglobulinemia |
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 |
D80.9 | Immunodeficiency with predominantly antibody defects, unspecified |
D81 | Combined immunodeficiencies |
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 |
D81.7 | Major histocompatibility complex class II deficiency |
D81.8 | Other combined immunodeficiencies |
D81.81 | Biotin-dependent carboxylase deficiency |
D81.810 | Biotinidase deficiency |
D81.818 | Other biotin-dependent carboxylase deficiency |
D81.819 | Biotin-dependent carboxylase deficiency, unspecified |
D81.89 | Other combined immunodeficiencies |
D81.9 | Combined immunodeficiency, unspecified |
D82 | Immunodeficiency associated with other major defects |
D82.0 | Wiskott-Aldrich syndrome |
D82.1 | Di George's syndrome |
D82.2 | Immunodeficiency with short-limbed stature |
D82.3 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
D82.4 | Hyperimmunoglobulin E [IgE] syndrome |
D82.8 | Immunodeficiency associated with other specified major defects |
D82.9 | Immunodeficiency associated with major defect, unspecified |
D83 | Common variable immunodeficiency |
D83.0 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
D83.1 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
D83.2 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
D83.8 | Other common variable immunodeficiencies |
D83.9 | Common variable immunodeficiency, unspecified |
D84 | Other immunodeficiencies |
D84.0 | Lymphocyte function antigen-1 [LFA-1] defect |
D84.1 | Defects in the complement system |
D84.8 | Other specified immunodeficiencies |
D84.9 | Immunodeficiency, unspecified |
D86 | Sarcoidosis |
D86.0 | Sarcoidosis of lung |
D86.1 | Sarcoidosis of lymph nodes |
D86.2 | Sarcoidosis of lung with sarcoidosis of lymph nodes |
D86.3 | Sarcoidosis of skin |
D86.8 | Sarcoidosis of other sites |
D86.81 | Sarcoid meningitis |
D86.82 | Multiple cranial nerve palsies in sarcoidosis |
D86.83 | Sarcoid iridocyclitis |
D86.84 | Sarcoid pyelonephritis |
D86.85 | Sarcoid myocarditis |
D86.86 | Sarcoid arthropathy |
D86.87 | Sarcoid myositis |
D86.89 | Sarcoidosis of other sites |
D86.9 | Sarcoidosis, unspecified |
D89 | Other disorders involving the immune mechanism, not elsewhere classified |
D89.0 | Polyclonal hypergammaglobulinemia |
D89.1 | Cryoglobulinemia |
D89.2 | Hypergammaglobulinemia, unspecified |
D89.3 | Immune reconstitution syndrome |
D89.8 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D89.81 | Graft-versus-host disease |
D89.810 | Acute graft-versus-host disease |
D89.811 | Chronic graft-versus-host disease |
D89.812 | Acute on chronic graft-versus-host disease |
D89.813 | Graft-versus-host disease, unspecified |
D89.82 | Autoimmune lymphoproliferative syndrome [ALPS] |
D89.89 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D89.9 | Disorder involving the immune mechanism, unspecified |