Q61.2 — Polycystic kidney, adult type

Q61.2

ICD-10 Chapter 17: Congenital & Genetic Disorders — illustrative image
Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00–QA1) — illustrative image

What this code means

Autosomal dominant polycystic kidney disease (adult type) causes many cysts to grow in the kidneys over a lifetime, gradually reducing function.

Also called: polycystic kidney disease, adpkd, adult polycystic kidney.

When this code is used

Used for polycystic kidney, adult type.

Where it sits in ICD-10-CM

Code Q61.2 belongs to Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders, which covers codes Q00–QA1 in the FY2027 ICD-10-CM tabular list. The official description above is copied verbatim from the CDC/NCHS FY2027 code file.

Related symptoms

Related anatomy

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Frequently asked questions

What is ICD-10-CM code Q61.2?

Q61.2 is the ICD-10-CM diagnosis code for “Polycystic kidney, adult type”. Autosomal dominant polycystic kidney disease (adult type) causes many cysts to grow in the kidneys over a lifetime, gradually reducing function.

When is code Q61.2 used?

Used for polycystic kidney, adult type. It belongs to Chapter 17 of ICD-10-CM (Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders).

This guide explains ICD-10-CM codes in plain language for patients, students and other readers. It is educational information only — not coding, billing or medical advice. The code recorded for any real encounter is assigned from the full clinical documentation by the treating team and qualified coders, and only they can decide which code fits a specific case.

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