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    v1.0.28
    OpenPayerBilling CodesCertain disorders involving the immune mechanismICD-10-CM d80-immunodeficiency-with-predominantly-antibody-defects
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    ICD-10-CM Code For Immunodeficiency With Predominantly Antibody Defects: Group Overview

    The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group D80 includes diagnoses of predominantly antibody-related immunodeficiencies such as agammaglobulinemia, hypogammaglobulinemia, and common variable immunodeficiency that impair humoral immunity. These ICD-10-CM diagnosis codes are used to document clinical scenarios involving recurrent infections, reduced immunoglobulin levels, and immune dysfunction, capturing disease severity and treatment complexity. Accurate coding within the ICD-10-CM D80 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.

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    ICD-10-CM D80: Immunodeficiency With Predominantly Antibody Defects Overview

    This group represents primary and secondary disorders characterized by impaired antibody production and humoral immune dysfunction affecting the immune system. It includes conditions such as agammaglobulinemia and common variable immunodeficiency that primarily target B-cell function and antibody-mediated immunity. Accurate coding is important because it documents disease severity and complexity, which impacts clinical management and reimbursement.

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    When to Use

    Use a code from this group when a patient has documented antibody deficiency demonstrated by low immunoglobulin levels, recurrent or unusual infections, or a known diagnosis of a B-cell related immunodeficiency. Assign codes that reflect the specific diagnosis and severity, including any documented complications or associated organ involvement.

    ICD-10-CM Codes

    10 rows

    ICD-10-CM CodeDescription
    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

    DRG Codes

    6 rows

    DRG CodeDescription
    808Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCC
    809Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC
    810Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCC
    814Reticuloendothelial and Immunity Disorders with MCC
    815Reticuloendothelial and Immunity Disorders with CC
    816Reticuloendothelial and Immunity Disorders without CC/MCC

    Typical Clinical Scenarios

    • An infant or young child with recurrent, severe bacterial otitis media, pneumonia, and failure to thrive is evaluated by pediatrics after multiple courses of antibiotics and poor response to routine immunizations; laboratory testing demonstrates markedly reduced serum immunoglobulin levels with poor vaccine antibody titers, prompting referral to immunology and initiation of immunoglobulin replacement therapy. Typical codes: D80.0, D80.1
    • An adult presents to the emergency department with an acute, high-grade fever and rapidly progressive sinopulmonary infection; history reveals long-standing recurrent sinopulmonary infections and laboratory assessment shows low B-cell counts and hypogammaglobulinemia, so admission is for intravenous antibiotics and prompt immunologic evaluation for a primary antibody deficiency. Typical codes: D80.3, D80.6
    • A middle-aged patient with a known antibody deficiency on chronic immunoglobulin replacement develops chronic diarrhea, weight loss, and new-onset autoimmune cytopenias; this visit is for management of complications of the underlying humoral immunodeficiency and optimization of therapy. Typical codes: D80.4, D80.5

    Related Codes

    D81-COMBINED-IMMUNODEFICIENCIES

    ICD-10-CM Code For Combined Immunodeficiencies: Group Overview

    D82-IMMUNODEFICIENCY-WITH-MAJOR-DEFECTS

    ICD-10-CM Code For Immunodeficiency Associated With Other Major Defects: Group Overview

    D83-COMMON-VARIABLE-IMMUNODEFICIENCY

    ICD-10-CM Code For Common Variable Immunodeficiency: Group Overview

    D84-OTHER-IMMUNODEFICIENCIES

    ICD-10-CM Code For Other Immunodeficiencies: Group Overview

    D86-SARCOIDOSIS

    ICD-10-CM Code For Sarcoidosis: Group Overview

    D89-OTHER-IMMUNE-MECHANISM-DISORDERS

    ICD-10-CM Code For Other Disorders Involving The Immune Mechanism Not Elsewhere Classified: Group Overview

    Frequently Asked Questions

    References

    1. 1.CPT® Codes and Descriptions. AAPC. Retrieved Aug 11, 2026.Maintains the CPT code set's official descriptions and guidelines, licensed from the American Medical Association, used as the definitional source for CPT codes on this page.
    2. 2.HCPCS Quarterly Update. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's quarterly release of HCPCS Level II codes and short/long descriptors, the source for HCPCS code definitions and update history.
    3. 3.ICD-10-CM Full Code List. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's complete ICD-10-CM diagnosis code list, used to cross-reference diagnosis codes associated with this procedure or service.
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