Agammaglobulinemia (acquired (secondary)) (nonfamilial)

"Agammaglobulinemia (acquired (secondary)) (nonfamilial)" References in the ICD-10-CM Index to Diseases and Injuries

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

Applicable Clinical Terms Definitions

Lymphopenia: Reduction in the number of lymphocytes.