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ICD-10 diagnosis code

Q61.1 Polycystic kidney, autosomal recessive

This page in Swedish

Q61.1 is the ICD-10 code for Polycystic kidney, autosomal recessive. 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 Q61.1 includes

Conditions and terms that are coded here.

  • Polycystic kidney, infantile type

Q61.1 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

Q61.1Polycystisk njure, autosomal recessiv

NorwayICD-10-NO

Q61.1Autosomal recessiv cystenyre

DenmarkICD-10-DK

DQ611Polycystisk nyresygdom med autosomal recessiv arvegang

FinlandICD-10-FI

Q61.1Lapsuustyyppinen munuaisten monirakkulatauti (polykystinen)

GermanyICD-10-GM

Q61.1Polyzystische Niere, autosomal-rezessiv

FranceICD-10-FR

Q61.1Rein polykystique, autosomique récessif

NetherlandsICD-10-NL

Q61.1polycystische nier, autosomaal recessief

United StatesICD-10-CM

Listed through more specific codes:

  • Q61.11Cystic dilatation of collecting ducts
  • Q61.19Other polycystic kidney, infantile 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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