Agammaglobulinemia (acquired (secondary)) (nonfamilial) - in the ICD-10-CM Index

Annotation Back-References in the 2025 ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "agammaglobulinemia (acquired (secondary)) (nonfamilial)"

  • Agammaglobulinemia (acquired (secondary)) (nonfamilial) - D80.1 Nonfamilial hypogammaglobulinemia

    • autosomal recessive (Swiss type) - D80.0 Hereditary hypogammaglobulinemia

    • Bruton's X-linked - D80.0 Hereditary hypogammaglobulinemia

    • common variable (CVAgamma) - D80.1 Nonfamilial hypogammaglobulinemia

    • congenital sex-linked - D80.0 Hereditary hypogammaglobulinemia

    • hereditary - D80.0 Hereditary hypogammaglobulinemia

    • lymphopenic - D81.9 Combined immunodeficiency, unspecified

    • Swiss type (autosomal recessive) - D80.0 Hereditary hypogammaglobulinemia

    • with

      • immunoglobulin-bearing B-lymphocytes - D80.1 Nonfamilial hypogammaglobulinemia

      • lymphopenia - D81.9 Combined immunodeficiency, unspecified

    • X-linked (with growth hormone deficiency) (Bruton) - D80.0 Hereditary hypogammaglobulinemia