ICD-10-CM · Chapter 3

D80..0 Hereditary hypogammaglobulinemia

Billable

← D80 — Immunodeficiency with predominantly antibody defects Chapter 3: D50-D89

Includes

Autosomal recessive agammaglobulinemia (Swiss type)
X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)

Last reviewed: September 2026