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ICD-10 Coding for Alport Syndrome(Q87.81)

Complete ICD-10-CM coding and documentation guide for Alport Syndrome. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

Hereditary NephritisAlport's Disease

Related ICD-10 Code Ranges

Complete code families applicable to Alport Syndrome

Q87.81Primary Range

Congenital malformation syndromes predominantly associated with short stature

Primary code for Alport syndrome, used when diagnosis is confirmed.

Nephrotic syndrome and other glomerular disorders

Used for documenting nephrotic syndrome and related kidney issues in Alport syndrome.

Other disorders of ear

Used for documenting hearing loss associated with Alport syndrome.

Other disorders of lens

Used for documenting ocular manifestations like anterior lenticonus in Alport syndrome.

Key Information: ICD-10 code for Alport syndrome

Essential facts and insights about Alport Syndrome

The ICD-10 code for Alport syndrome is Q87.81, used when confirmed by genetic testing.

Primary ICD-10-CM Code for alport syndrome

Alport syndrome
Billable Code

Decision Criteria

clinical Criteria

  • Presence of genetic mutation in COL4A3, COL4A4, or COL4A5.

documentation Criteria

  • Documented family history and clinical symptoms consistent with Alport syndrome.

Applicable To

  • Alport syndrome with confirmed genetic mutation

Excludes

  • Other specified congenital malformations

Clinical Validation Requirements

  • Genetic test results showing COL4A3, COL4A4, or COL4A5 variants
  • Family history of Alport syndrome
  • Renal biopsy findings

Code-Specific Risks

  • Risk of audit if used without supporting genetic or biopsy documentation.

Coding Notes

  • Ensure genetic confirmation or clinical criteria are documented to support coding.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Nephrotic syndrome

N04.9
Use for documenting nephrotic syndrome with proteinuria >3.5g/day.

Sensorineural hearing loss

H91.3
Use when hearing loss is documented with audiometry results.

Anterior lenticonus

H27.1
Use for ocular manifestations confirmed by ophthalmology exam.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Nephrotic syndrome, unspecified

N04.9
Use for nephrotic syndrome when proteinuria is documented.

Sensorineural hearing loss, bilateral

H91.3
Use when audiometry confirms bilateral sensorineural hearing loss.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Alport Syndrome to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code Q87.81.

Impact

Clinical: May lead to incomplete clinical picture., Regulatory: Non-compliance with documentation standards., Financial: Potential claim denials for incomplete documentation.

Mitigation Strategy

Ensure audiometry results are included in the patient record., Verify documentation before coding.

Impact

Reimbursement: May lead to denied claims due to lack of specificity., Compliance: Non-compliance with ICD-10 coding guidelines., Data Quality: Decreases accuracy of health records.

Mitigation Strategy

Specify 'Alport syndrome' and include genetic testing results.

Impact

Risk of audit if genetic testing is not documented when coding for Alport syndrome.

Mitigation Strategy

Ensure all genetic testing results are included in the patient's medical record.

Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.

Frequently Asked Questions

Common questions about ICD-10 coding for Alport Syndrome, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Alport Syndrome

Use these documentation templates to ensure complete and accurate documentation for Alport Syndrome. These templates include all required elements for proper coding and billing.

Nephrology Progress Note

Specialty: Nephrology

Required Elements

  • Family history of Alport syndrome
  • Genetic test results
  • Renal biopsy findings
  • Audiometry results

Example Documentation

Patient diagnosed with Alport syndrome confirmed by COL4A5 mutation. Persistent hematuria and proteinuria documented. Bilateral sensorineural hearing loss confirmed by audiometry.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has hereditary nephritis.
Good Documentation Example
X-linked Alport syndrome confirmed by COL4A5 mutation. Persistent microscopic hematuria since age 5, UPCR 0.8, bilateral high-frequency hearing loss at 2000-8000 Hz diagnosed at age 12.
Explanation
The good example provides specific genetic confirmation and detailed clinical findings.

Need help with ICD-10 coding for Alport Syndrome? Ask your questions below.

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