2026 ICD-10-CM Diagnosis Code Q61.11Cystic dilatation of collecting ducts

ICD-10-CM Codes›Q00-Q99›Q60-Q64›Q61

ICD-10-CM Q61.11
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

Q61.11 is a billable ICD-10-CM diagnosis code for cystic dilatation of collecting ducts. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 698 through 700. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Genitourinary congenital anomalies.

Code Identity

ICD-10-CM Code
Q61.11
Billable Status
Yes — Valid for Submission
Code Describes
Cystic dilatation of collecting ducts
Short Description
Cystic dilatation of collecting ducts
Same as the full description in the CMS dataset.
Parent Code
Q61.1
Polycystic kidney, infantile type

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ60-Q64Congenital malformations of the urinary system
CategoryQ61Cystic kidney disease
This CodeQ61.11Cystic dilatation of collecting ducts

Present on Admission (POA)Billing

Q61.11 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Cyst(colloid) (mucous) (simple) (retention)
      • congenital NEC
        • kidney
          • more than one (multiple)
            • specified as polycystic
              • infantile type NEC
                • collecting duct dilation
    • Cyst(colloid) (mucous) (simple) (retention)
      • kidney
        • more than one (multiple)
          • specified as polycystic
            • infantile type (autosomal recessive) NEC
              • collecting duct dilation
    • Cystic
      • kidney (congenital)
        • infantile type NEC
          • collecting duct dilatation
    • Degeneration, degenerative
      • kidney
        • polycystic
          • infantile type (autosomal recessive) NEC
            • collecting duct dilatation
    • Disease, diseased
      • kidney (functional) (pelvis)
        • polycystic
          • childhood type NEC
            • collecting duct dilatation
    • Disease, diseased
      • polycystic
        • kidney or renal
          • childhood type NEC
            • collecting duct dilatation
    • Disease, diseased
      • renal (functional) (pelvis)
        • polycystic (congenital)
          • childhood type NEC
            • collecting duct dilatation

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR MAL003
Genitourinary congenital anomalies
Default principal diagnosis: inpatient Yes · outpatient Yes

Patient EducationClinical

Kidney Cysts

A cyst is a fluid-filled sac. You may get simple kidney cysts as you age; they are usually harmless. There are also some diseases which cause kidney cysts. One type is polycystic kidney disease (PKD). It runs in families. In PKD, many cysts grow in the kidneys. This can enlarge the kidneys and make them work poorly.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q61.11 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
753.14 Polycyst kid-autosom rec
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About Q61.11Overview

Is Q61.11 (Polycystic kidney, infantile type) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report cystic dilatation of collecting ducts on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does Q61.11 group to?

When cystic dilatation of collecting ducts is the principal diagnosis on an inpatient stay, it groups to MS-DRG 698, 699, 700, with relative weights from 0.6899 to 1.6544 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q61.11 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for cystic dilatation of collecting ducts on inpatient claims.

What is the ICD-9 equivalent of Q61.11?

Under the General Equivalence Mappings, cystic dilatation of collecting ducts converts to ICD-9-CM 753.14 (polycyst kid-autosom rec). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.