ICD-10-CM D50 to D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism: one chapter of ICD-10-CM.
398 codes · page 7 of 8 · every chapter
Nonfamilial hypogammaglobulinemia D80.1 Selective deficiency of immunoglobulin A [IgA] D80.2 Selective deficiency of immunoglobulin G [IgG] subclasses D80.3 Selective deficiency of immunoglobulin M [IgM] D80.4 Immunodeficiency with increased immunoglobulin M [IgM] D80.5 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia D80.6 Transient hypogammaglobulinemia of infancy D80.7 Other immunodeficiencies with predominantly antibody defects Other immunodeficiencies with predominantly antibody defects D80.8 Immunodeficiency with predominantly antibody defects, unspecified D80.9 Combined immunodeficiencies D81 Severe combined immunodeficiency [SCID] with reticular dysgenesis D81.0 Severe combined immunodeficiency w low T- and B-cell numbers Severe combined immunodeficiency [SCID] with low T- and B-cell numbers D81.1 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers D81.2 Adenosine deaminase [ADA] deficiency D81.3 Adenosine deaminase deficiency, unspecified D81.30 Severe combined immunodeficiency due to adenosine deaminase deficiency D81.31 Adenosine deaminase 2 deficiency D81.32 Other adenosine deaminase deficiency D81.39 Nezelof's syndrome D81.4 Purine nucleoside phosphorylase [PNP] deficiency D81.5 Major histocompatibility complex class I deficiency D81.6 Major histocompatibility complex class II deficiency D81.7 Other combined immunodeficiencies D81.8 Biotin-dependent carboxylase deficiency D81.81 Biotinidase deficiency D81.810 Other biotin-dependent carboxylase deficiency D81.818 Biotin-dependent carboxylase deficiency, unspecified D81.819 Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] D81.82 Other combined immunodeficiencies D81.89 Combined immunodeficiency, unspecified D81.9 Immunodeficiency associated with other major defects D82 Wiskott-Aldrich syndrome D82.0 Di George's syndrome D82.1 Immunodeficiency with short-limbed stature D82.2 Immunodeficiency following hereditary defective response to Epstein-Barr virus D82.3 Hyperimmunoglobulin E [IgE] syndrome D82.4 Immunodeficiency associated with other specified major defects D82.8 Immunodeficiency associated with major defect, unspecified D82.9 Common variable immunodeficiency D83 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function D83.0 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders D83.1 Common variable immunodeficiency with autoantibodies to B- or T-cells D83.2 Other common variable immunodeficiencies D83.8 Common variable immunodeficiency, unspecified D83.9 Other immunodeficiencies D84 Lymphocyte function antigen-1 [LFA-1] defect D84.0 Defects in the complement system D84.1 Other specified immunodeficiencies D84.8 Immunodeficiency due to conditions classified elsewhere D84.81 Immunodeficiency due to drugs and external causes D84.82