Back to HomeBeta

ICD-10 Coding for Duchenne Muscular Dystrophy(G71.01)

Complete ICD-10-CM coding and documentation guide for Duchenne Muscular Dystrophy. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

DMDDuchenne's Muscular Dystrophy

Related ICD-10 Code Ranges

Complete code families applicable to Duchenne Muscular Dystrophy

G71.0-G71.9Primary Range

Primary muscular disorders

This range includes codes for various muscular dystrophies, with G71.01 specifically for Duchenne or Becker muscular dystrophy.

Key Information: ICD-10 code for Duchenne's muscular dystrophy

Essential facts and insights about Duchenne Muscular Dystrophy

The ICD-10 code for Duchenne's muscular dystrophy is G71.01, used when genetic testing confirms the condition.

Primary ICD-10-CM Code for duchenne's muscular dystrophy

Duchenne or Becker muscular dystrophy
Billable Code

Decision Criteria

clinical Criteria

  • Confirmed DMD gene mutation via genetic testing

documentation Criteria

  • Detailed documentation of muscle weakness and genetic test results

Applicable To

  • Duchenne muscular dystrophy
  • Becker muscular dystrophy

Excludes

  • Limb-girdle muscular dystrophy (G71.03)

Clinical Validation Requirements

  • Genetic testing confirming DMD gene mutation
  • Elevated creatine kinase (CK) levels
  • Muscle biopsy showing absent dystrophin

Code-Specific Risks

  • Misclassification if genetic testing is not documented
  • Incorrect use if symptoms are not specific to Duchenne or Becker

Coding Notes

  • Ensure genetic testing results are documented to support the use of G71.01.

Ancillary Codes

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

Cardiomyopathy in diseases classified elsewhere

I43.1
Use to specify cardiac involvement in Duchenne muscular dystrophy.

Contracture of muscle, unspecified site

M62.40
Use to document specific muscle contractures associated with Duchenne.

Differential Codes

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

Limb-girdle muscular dystrophy

G71.03
Preserved facial muscles and normal dystrophin levels differentiate it from Duchenne.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Duchenne Muscular Dystrophy to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code G71.01.

Impact

Clinical: May lead to misdiagnosis or inappropriate treatment., Regulatory: Non-compliance with documentation standards., Financial: Potential for denied claims due to insufficient documentation.

Mitigation Strategy

Ensure all genetic test results are included in the patient's medical record., Train staff on the importance of detailed genetic documentation.

Impact

Reimbursement: Incorrect coding may lead to denied claims or reduced reimbursement., Compliance: Non-compliance with coding guidelines., Data Quality: Impacts the accuracy of patient records and data analytics.

Mitigation Strategy

Always use G71.01 when genetic testing confirms Duchenne muscular dystrophy.

Impact

Lack of genetic test documentation may lead to audit issues.

Mitigation Strategy

Ensure all genetic test results are documented and easily accessible.

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 Duchenne Muscular Dystrophy, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Duchenne Muscular Dystrophy

Use these documentation templates to ensure complete and accurate documentation for Duchenne Muscular Dystrophy. These templates include all required elements for proper coding and billing.

Neurology Clinic Visit for DMD

Specialty: Neurology

Required Elements

  • Patient history
  • Genetic test results
  • CK levels
  • Functional status
  • Cardiac evaluation

Example Documentation

Patient with Duchenne MD confirmed by genetic testing. CK 15,000 U/L. Wheelchair-dependent since age 10. Cardiomyopathy present.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient with MD. Weakness worsening.
Good Documentation Example
Patient with Duchenne MD (G71.01) confirmed by DMD exon 51 deletion. CK 12,500 U/L. Progressive quadriceps weakness, wheelchair-dependent since age 11.
Explanation
The good example provides specific genetic confirmation, CK levels, and detailed functional status.

Need help with ICD-10 coding for Duchenne Muscular Dystrophy? Ask your questions below.

Ask about any ICD-10 CM code, or paste a medical note

We build tools for
clinician happiness.

Learn More at Freed.ai
Back to HomeBeta

Built by Freed

Try Freed for free for 7 days.

Learn more