ICD-10 Logo
ICDxICD-10 Medical Coding
ICD-10 Logo
ICDxICD-10 Medical Coding
ICD 10 CodesDiagnoses
ICD 10 CodesDiagnoses
ICD-10 Logo
ICDxICD-10 Medical Coding

Comprehensive ICD-10-CM code reference with AI-powered search capabilities.

© 2025 ICD Code Compass. All rights reserved.

Browse

  • All Chapters
  • All Categories
  • Diagnoses

Tools

  • AI Code Search
ICD-10-CM codes are maintained by the CDC and CMS. This tool is for reference purposes only.
v1.0.0
ICD-10 Guide
ICD-10 CodesQ61.2

Q61.2

Billable

Polycystic kidney, adult type

BILLABLE STATUSYes
IMPLEMENTATION DATEOctober 1, 2015
LAST UPDATED09/11/2025

Code Description

ICD-10 Q61.2 is a billable code used to indicate a diagnosis of polycystic kidney, adult type.

Key Diagnostic Point:

Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The adult type, also known as autosomal dominant polycystic kidney disease (ADPKD), typically manifests in adulthood, although cysts can begin to form in childhood. This condition leads to enlarged kidneys and can result in hypertension, hematuria, and renal insufficiency. Patients may experience abdominal or flank pain due to the size of the kidneys or complications from cysts. The disease is often associated with mutations in the PKD1 or PKD2 genes, which are crucial for normal kidney function. Diagnosis is typically confirmed through imaging studies such as ultrasound or CT scans, which reveal the presence of cysts. Management may include controlling blood pressure, pain management, and, in advanced cases, dialysis or kidney transplantation. Understanding the genetic basis and familial patterns of this condition is essential for effective patient management and genetic counseling.

Code Complexity Analysis

Complexity Rating: Medium

Medium Complexity

Complexity Factors

  • Differentiating between types of polycystic kidney disease (ADPKD vs. ARPKD)
  • Understanding the genetic implications and family history requirements
  • Interpreting imaging results for accurate diagnosis
  • Managing co-existing conditions such as hypertension

Audit Risk Factors

  • Inadequate documentation of family history and genetic testing results
  • Failure to specify the type of polycystic kidney disease
  • Misclassification of cystic kidney disease types
  • Lack of supporting imaging documentation

Specialty Focus

Medical Specialties

Pediatrics

Documentation Requirements

Detailed family history, growth and development assessments, and imaging results.

Common Clinical Scenarios

Pediatric patients presenting with abdominal pain, hypertension, or urinary issues.

Billing Considerations

Consideration of early onset symptoms and the need for genetic counseling in families.

Genetics

Documentation Requirements

Genetic testing results, family pedigree, and counseling notes.

Common Clinical Scenarios

Patients undergoing genetic counseling for family planning or those with a family history of PKD.

Billing Considerations

Understanding the inheritance patterns and implications for family members.

Coding Guidelines

Inclusion Criteria

Use Q61.2 When
  • Follow the ICD
  • CM guidelines for coding congenital malformations, ensuring accurate documentation of the condition's nature, associated symptoms, and any genetic testing performed

Exclusion Criteria

Do NOT use Q61.2 When
No specific exclusions found.

Related ICD-10 Codes

Related CPT Codes

76700CPT Code

Ultrasound, abdomen, complete

Clinical Scenario

Used to evaluate renal cysts in suspected cases of PKD.

Documentation Requirements

Document indications for ultrasound and findings.

Specialty Considerations

Pediatric specialists may require additional documentation for growth assessments.

ICD-10 Impact

Diagnostic & Documentation Impact

Enhanced Specificity

ICD-10 Improvements

The transition to ICD-10 has allowed for more specific coding of congenital conditions, improving the accuracy of data collection and reimbursement processes for conditions like polycystic kidney disease.

ICD-9 vs ICD-10

The transition to ICD-10 has allowed for more specific coding of congenital conditions, improving the accuracy of data collection and reimbursement processes for conditions like polycystic kidney disease.

Reimbursement & Billing Impact

reimbursement processes for conditions like polycystic kidney disease.

Resources

Clinical References

  • •
    National Kidney Foundation

Coding & Billing References

  • •
    National Kidney Foundation

Frequently Asked Questions

What is the difference between ADPKD and ARPKD?

ADPKD is typically diagnosed in adulthood and is inherited in an autosomal dominant pattern, while ARPKD is diagnosed in infancy or early childhood and is inherited in an autosomal recessive pattern. The clinical manifestations and management strategies differ significantly between the two.