Online 2016 ICD-10-CM · Tabular List · Alpha Index · ICD-9/ICD-10 conversion · ICD-10-PCS

D80Immunodeficiency with predominantly antibody defects
D80.0Hereditary hypogammaglobulinemia
D80.1Nonfamilial hypogammaglobulinemia
D80.2Selective deficiency of immunoglobulin A [IgA]
D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
D80.4Selective deficiency of immunoglobulin M [IgM]
D80.5Immunodeficiency with increased immunoglobulin M [IgM]
D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D80.7Transient hypogammaglobulinemia of infancy
D80.8Other immunodeficiencies with predominantly antibody defects
D80.9Immunodeficiency with predominantly antibody defects, unspecified
D81Combined immunodeficiencies
D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D81.3Adenosine deaminase [ADA] deficiency
D81.4Nezelof's syndrome
D81.5Purine nucleoside phosphorylase [PNP] deficiency
D81.6Major histocompatibility complex class I deficiency
D81.7Major histocompatibility complex class II deficiency
D81.8Other combined immunodeficiencies
D81.81Biotin-dependent carboxylase deficiency
D81.810Biotinidase deficiency
D81.818Other biotin-dependent carboxylase deficiency
D81.819Biotin-dependent carboxylase deficiency, unspecified
D81.89Other combined immunodeficiencies
D81.9Combined immunodeficiency, unspecified
D82Immunodeficiency associated with other major defects
D82.0Wiskott-Aldrich syndrome
D82.1Di George's syndrome
D82.2Immunodeficiency with short-limbed stature
D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
D82.4Hyperimmunoglobulin E [IgE] syndrome
D82.8Immunodeficiency associated with other specified major defects
D82.9Immunodeficiency associated with major defect, unspecified
D83Common variable immunodeficiency
D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
D83.8Other common variable immunodeficiencies
D83.9Common variable immunodeficiency, unspecified
D84Other immunodeficiencies
D84.0Lymphocyte function antigen-1 [LFA-1] defect
D84.1Defects in the complement system
D84.8Other specified immunodeficiencies
D84.9Immunodeficiency, unspecified
D86.0Sarcoidosis of lung
D86.1Sarcoidosis of lymph nodes
D86.2Sarcoidosis of lung with sarcoidosis of lymph nodes
D86.3Sarcoidosis of skin
D86.8Sarcoidosis of other sites
D86.81Sarcoid meningitis
D86.82Multiple cranial nerve palsies in sarcoidosis
D86.83Sarcoid iridocyclitis
D86.84Sarcoid pyelonephritis
D86.85Sarcoid myocarditis
D86.86Sarcoid arthropathy
D86.87Sarcoid myositis
D86.89Sarcoidosis of other sites
D86.9Sarcoidosis, unspecified
D89Other disorders involving the immune mechanism, not elsewhere classified
D89.0Polyclonal hypergammaglobulinemia
D89.2Hypergammaglobulinemia, unspecified
D89.3Immune reconstitution syndrome
D89.8Other specified disorders involving the immune mechanism, not elsewhere classified
D89.81Graft-versus-host disease
D89.810Acute graft-versus-host disease
D89.811Chronic graft-versus-host disease
D89.812Acute on chronic graft-versus-host disease
D89.813Graft-versus-host disease, unspecified
D89.82Autoimmune lymphoproliferative syndrome [ALPS]
D89.89Other specified disorders involving the immune mechanism, not elsewhere classified
D89.9Disorder involving the immune mechanism, unspecified