Q61.2 is the ICD-10 code for Polycystic kidney, autosomal dominant. It is a four-character subcategory of Q61 (Cystic kidney disease), the most specific level in the WHO edition. It belongs to the block Q60–Q64 (Congenital malformations of the urinary system) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.
- Code type
- Subcategory (4 characters)
- Chapter
- XVII · Q00–Q99
- Classification
- WHO ICD-10, 2019 version
What Q61.2 includes
Conditions and terms that are coded here.
- Polycystic kidney, adult type
Q61.2 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q61.2Autosomal dominant cystenyre
DQ612Polycystisk nyresygdom med autosomal dominant arvegang
Q61.2Aikuistyyppinen munuaisten monirakkulatauti (polykystinen)
Q61.2Polyzystische Niere, autosomal-dominant
Q61.2Rein polykystique, autosomique dominant
Q61.2polycystische nier, autosomaal dominant
Q61.2Polycystic kidney, adult type
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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