Immunodeficiency - in the ICD-10-CM Index

Browse the ICD-10-CM codes with references applicable to the clinical term "immunodeficiency"

• Immunodeficiency - D84.9 Immunodeficiency, unspecified

  • antibody with

    • hyperimmunoglobulinemia - D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia

    • near-normal immunoglobulins - D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia

  • autosomal recessive, Swiss type - D80.0 Hereditary hypogammaglobulinemia

  • combined - D81.9 Combined immunodeficiency, unspecified

    • biotin-dependent carboxylase - D81.819 Biotin-dependent carboxylase deficiency, unspecified

      • biotinidase - D81.810 Biotinidase deficiency

      • holocarboxylase synthetase - D81.818 Other biotin-dependent carboxylase deficiency

      • specified type NEC - D81.818 Other biotin-dependent carboxylase deficiency

    • severe (SCID) - D81.9 Combined immunodeficiency, unspecified

      • with

        • low or normal B-cell numbers - D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers

        • low T- and B-cell numbers - D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers

        • reticular dysgenesis - D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis

    • specified type NEC - D81.89 Other combined immunodeficiencies

  • common variable - D83.9 Common variable immunodeficiency, unspecified

    • specified type NEC - D83.8 Other common variable immunodeficiencies

    • with

      • abnormalities of B-cell numbers and function - D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

      • autoantibodies to B- or T-cells - D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells

      • immunoregulatory T-cell disorders - D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders

  • due to

    • conditions classified elsewhere - D84.81 Immunodeficiency due to conditions classified elsewhere

    • drugs - D84.821 Immunodeficiency due to drugs

    • external causes - D84.822 Immunodeficiency due to external causes

    • medication (current or past) - D84.821 Immunodeficiency due to drugs

  • following hereditary defective response to Epstein-Barr virus (EBV) - D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus

  • selective, immunoglobulin

    • A (IgA) - D80.2 Selective deficiency of immunoglobulin A [IgA]

    • G (IgG) (subclasses) - D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses

    • M (IgM) - D80.4 Selective deficiency of immunoglobulin M [IgM]

  • severe combined (SCID) - D81.9 Combined immunodeficiency, unspecified

    • due to adenosine deaminase deficiency - D81.31 Severe combined immunodeficiency due to adenosine deaminase deficiency

  • specified type NEC - D84.89 Other immunodeficiencies

  • with

    • adenosine-deaminase deficiency - See Also: Deficiency, adenosine deaminase; - D81.30 Adenosine deaminase deficiency, unspecified

    • antibody defects - D80.9 Immunodeficiency with predominantly antibody defects, unspecified

      • specified type NEC - D80.8 Other immunodeficiencies with predominantly antibody defects

    • hyperimmunoglobulinemia - D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia

    • increased immunoglobulin M (IgM) - D80.5 Immunodeficiency with increased immunoglobulin M [IgM]

    • major defect - D82.9 Immunodeficiency associated with major defect, unspecified

      • specified type NEC - D82.8 Immunodeficiency associated with other specified major defects

    • partial albinism - D82.8 Immunodeficiency associated with other specified major defects

    • short-limbed stature - D82.2 Immunodeficiency with short-limbed stature

    • thrombocytopenia and eczema - D82.0 Wiskott-Aldrich syndrome

  • X-linked, with increased IgM - D80.5 Immunodeficiency with increased immunoglobulin M [IgM]