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Home/Diagnosis/ICD-10 Coding for Autosomal Dominant Polycystic Kidney Disease

ICD-10 Coding for Autosomal Dominant Polycystic Kidney Disease

Q61.2
Q61.3

Complete ICD-10-CM coding and documentation guide for icd-10 coding for autosomal dominant polycystic kidney disease includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
ADPKD
Polycystic Kidney Disease Type 1
Polycystic Kidney Disease Type 2
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Key Information: ICD-10 Coding for Autosomal Dominant Polycystic Kidney Disease

Essential facts and insights about ICD-10 Coding for Autosomal Dominant Polycystic Kidney Disease

Use ICD-10 code Q61.2 for autosomal dominant polycystic kidney disease, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Autosomal dominant polycystic kidney disease

Billable Code
Q61.2
Billable

Diagnostic Criteria

clinical:
  • • Presence of ≥3 bilateral renal cysts and family history
coding:
  • • Confirmed genetic testing for PKD1 or PKD2

Applicable To

  • • Confirmed ADPKD with genetic testing
  • • ≥3 bilateral renal cysts with family history

Important Notes

  • • Ensure documentation supports the use of Q61.2 with genetic or imaging evidence.

Polycystic kidney, unspecified

Billable Code
Q61.3
Billable

Applicable To

  • • Polycystic kidney disease without specified inheritance pattern

Important Notes

  • • Avoid using Q61.3 when specific diagnosis can be confirmed.
Ancillary Codes

Additional codes that may be used with this diagnosis

N28.89

Other specified disorders of kidney

Use for complications such as cyst infection or hemorrhage.

Frequently Asked Questions

What is the ICD-10 code for autosomal dominant polycystic kidney disease?

The ICD-10 code for autosomal dominant polycystic kidney disease is Q61.2, used when the condition is confirmed through genetic testing or clinical criteria.

How is ADPKD diagnosed?

ADPKD is diagnosed through imaging showing multiple bilateral renal cysts, family history, and genetic testing for PKD1 or PKD2 mutations.

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