Q61.1

Polycystic kidney, autosomal recessive

Coding guidance (WHO 2019)

Polycystic kidney, infantile type

Sibling codes

Q61Cystic kidney disease Q61.0Congenital single renal cyst Q61.2Polycystic kidney, autosomal dominant Q61.3Polycystic kidney, unspecified Q61.4Renal dysplasia Q61.5Medullary cystic kidney Q61.8Other cystic kidney diseases Q61.9Cystic kidney disease, unspecified

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