D89.0 is the ICD-10 code for Polyclonal hypergammaglobulinaemia. It is a four-character subcategory of D89 (Other disorders involving the immune mechanism, not elsewhere classified), 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 D89.0 includes
Conditions and terms that are coded here.
- Benign hypergammaglobulinaemic purpura
- Polyclonal gammopathy NOS
D89.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D89.0Polyklonal hypergammaglobulinemi
DD890Polyklonal hypergammaglobulinæmi
- DD890APolyklonal gammopati UNS
- DD890BBenign hypergammaglobulinæmisk purpura
D89.0Polyklonaalinen hypergammaglobulinemia
D89.0Polyklonale Hypergammaglobulinämie
D89.0Hypergammaglobulinémie polyclonale
D89.0polyklonale hypergammaglobulinemie
D89.0Polyclonal hypergammaglobulinemia
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.
Look up another code
Stop looking codes up by hand
Docdemic listens to the consultation, writes the note and suggests the diagnosis and procedure codes that fit it, each one checked against your country’s official code list.
Try Docdemic free