Q61.1Header code — not billable
Polycystic kidney, infantile type
- Chapter
- 17. Congenital malformations, deformations and chromosomal abnormalities
- Category
- Q61
- Effective date
- October 1, 2026
Related codes in category Q61
Q61Cystic kidney diseaseQ61.0Congenital renal cystQ61.00Congenital renal cyst, unspecifiedYesQ61.01Congenital single renal cystYesQ61.02Congenital multiple renal cystsYesQ61.11Cystic dilatation of collecting ductsYesQ61.19Other polycystic kidney, infantile typeYesQ61.2Polycystic kidney, adult typeYesQ61.3Polycystic kidney, unspecifiedYesQ61.4Renal dysplasiaYesQ61.5Medullary cystic kidneyYesQ61.8Other cystic kidney diseasesYes
Frequently asked questions
What is ICD-10 code Q61.1?
Q61.1 is an ICD-10-CM diagnosis code for Polycystic kidney, infantile type.
Is Q61.1 a billable code?
No. Q61.1 is a category/header code, not billable on its own — use one of its more specific child codes instead.
What ICD-10-CM chapter is Q61.1 in?
Q61.1 falls under Chapter 17: Congenital malformations, deformations and chromosomal abnormalities.
When did Q61.1 become effective?
Q61.1 has been effective since October 1, 2026, per the CMS/CDC ICD-10-CM annual release.
What other codes are related to Q61.1?
Q61.1 belongs to category Q61, which includes 12 other codes — see the related codes list on this page.
ICD-10-CM data maintained by CDC/CMS (public domain). Always verify codes with authoritative sources before making coding or billing decisions.