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ICD-10 Coding for Cerebellar Ataxia(G11.10, G11.11, G11.3)

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

Also known as:

Hereditary AtaxiaSpinocerebellar AtaxiaFriedreich's Ataxia

Related ICD-10 Code Ranges

Complete code families applicable to Cerebellar Ataxia

G11.0-G11.9Primary Range

Hereditary ataxia

This range includes various forms of hereditary ataxia, including early-onset and specific genetic types.

Symptoms involving nervous and musculoskeletal systems

This range includes codes for symptoms like unsteadiness on feet, which may be used when specific ataxia types are not confirmed.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
G11.10Early-onset cerebellar ataxia, unspecifiedUse when early-onset cerebellar ataxia is diagnosed but specific type is not identified.
  • Clinical documentation excluding Friedreich ataxia
  • Early onset of symptoms
G11.11Friedreich ataxiaUse when genetic testing confirms Friedreich ataxia.
  • Genetic testing confirming FXN gene mutation
  • Presence of cardiomyopathy and pes cavus
G11.3Cerebellar ataxia with defective DNA repairUse when cerebellar ataxia is due to a genetic disorder affecting DNA repair.
  • Documentation of genetic disorder affecting DNA repair
  • Elevated alpha-fetoprotein levels

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for cerebellar ataxia

Essential facts and insights about Cerebellar Ataxia

The ICD-10 code for cerebellar ataxia includes G11.10 for unspecified early-onset and G11.11 for Friedreich ataxia.

Primary ICD-10-CM Codes for cerebellar ataxia

Early-onset cerebellar ataxia, unspecified
Billable Code

Decision Criteria

clinical Criteria

  • Early onset of cerebellar symptoms without specific genetic confirmation

Applicable To

  • Unspecified early-onset cerebellar ataxia

Excludes

Clinical Validation Requirements

  • Clinical documentation excluding Friedreich ataxia
  • Early onset of symptoms

Code-Specific Risks

  • Risk of undercoding if specific type is known

Coding Notes

  • Ensure documentation excludes Friedreich ataxia.

Ancillary Codes

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

Unsteadiness on feet

R26.81
Use only if gait instability persists after addressing primary ataxia.

Differential Codes

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

Friedreich ataxia

G11.11
Requires genetic confirmation of FXN gene mutation.

Early-onset cerebellar ataxia, unspecified

G11.10
Use G11.10 if genetic testing for Friedreich ataxia is negative or not performed.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Cerebellar Ataxia to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code G11.10.

Impact

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

Mitigation Strategy

Ensure genetic testing is ordered and results documented., Educate staff on documentation standards.

Impact

Reimbursement: May lead to incorrect reimbursement levels., Compliance: Non-compliance with coding guidelines., Data Quality: Decreases accuracy of clinical data.

Mitigation Strategy

Ensure documentation explicitly excludes Friedreich ataxia before using G11.10.

Impact

Reimbursement: Potential for duplicate billing., Compliance: Violation of coding guidelines., Data Quality: Redundant data entry.

Mitigation Strategy

Avoid using R26.81 if ataxia is already coded with G11.11.

Impact

Lack of documentation for genetic testing in hereditary ataxia cases.

Mitigation Strategy

Implement mandatory documentation checks for genetic testing results.

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 Cerebellar Ataxia, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Cerebellar Ataxia

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

Friedreich Ataxia Diagnosis

Specialty: Neurology

Required Elements

  • Genetic testing results
  • SARA score
  • MRI findings

Example Documentation

25yo male with progressive gait instability, bilateral pes cavus, and hypertrophic cardiomyopathy. Genetic testing: FXN gene shows homozygous GAA repeats (98/1200). SARA score 22/40.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient has balance problems.
Good Documentation Example
Patient exhibits truncal titubation and dysmetria on finger-nose testing, SARA score 18/40.
Explanation
The good example provides specific clinical findings and a standardized assessment score.

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