D80.0 is the ICD-10 code for Hereditary hypogammaglobulinaemia. It is a four-character subcategory of D80 (Immunodeficiency with predominantly antibody defects), the most specific level in the WHO edition. It belongs to the block D80–D89 (Certain disorders involving the immune mechanism) in Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Code type
- Subcategory (4 characters)
- Chapter
- III · D50–D89
- Classification
- WHO ICD-10, 2019 version
What D80.0 includes
Conditions and terms that are coded here.
- Autosomal recessive agammaglobulinaemia (Swiss type)
- X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)
D80.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D80.0Hereditär hypogammaglobulinemi
- D80.0AHereditär agammaglobulinemi, könsbunden
- D80.0BHereditär agammaglobulinemi, autosomalt recessiv
- D80.0WAnnan hereditär hypogammaglobulinemi
D80.0Arvelig hypogammaglobulinemi
DD800Arvelig hypogammaglobulinæmi
- DD800AAutosomal recessiv agammaglobulinæmi (Swiss type)
- DD800BX-bundet agammaglobulinæmi med væksthormonmangel
D80.0Perinnöllinen hypogammaglobulinemia
D80.0Hereditäre Hypogammaglobulinämie
D80.0Hypogammaglobulinémie héréditaire
D80.0hereditaire hypogammaglobulinemie
D80.0Hereditary hypogammaglobulinemia
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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