D80.1 is the ICD-10 code for Nonfamilial 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 D80.1 includes
Conditions and terms that are coded here.
- Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes
- Common variable agammaglobulinaemia [CVAgamma]
- Hypogammaglobulinaemia NOS
D80.1 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D80.1Ikke-familiær hypogammaglobulinemi
DD801Ikke-familiær hypogammaglobulinæmi
- DD801AHypogammaglobulinæmi UNS
- DD801BAgammaglobulinæmi med immunglobulinbærende B-lymfocyter
- DD801CCommon variable agammaglobulinemia (CVA-gamma)
D80.1Ei-suvuittainen hypogammaglobulinemia
D80.1Nichtfamiliäre Hypogammaglobulinämie
D80.1Hypogammaglobulinémie non familiale
D80.1niet-familiale hypogammaglobulinemie
D80.1Nonfamilial 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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