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ICD-10 Coding for Spinal Muscular Atrophy(G12.0, G12.1, G12.9)

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

Also known as:

SMA5q SMAProximal Spinal Muscular Atrophy

Related ICD-10 Code Ranges

Complete code families applicable to Spinal Muscular Atrophy

G12.0-G12.9Primary Range

Spinal muscular atrophy and related syndromes

This range covers all types of spinal muscular atrophy, including infantile and other inherited forms.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
G12.0Infantile spinal muscular atrophy, type I [Werdnig-Hoffmann]Use for infantile-onset SMA with genetic confirmation and characteristic clinical presentation.
  • Homozygous SMN1 deletion
  • 1-2 SMN2 copies
  • Absent motor milestones
G12.1Other inherited spinal muscular atrophyUse for late-onset SMA with confirmed genetic testing.
  • Confirmed SMN1 mutation
  • 3 or more SMN2 copies
  • Late-onset presentation
G12.9Spinal muscular atrophy, unspecifiedUse only when genetic testing is pending.
  • Pending genetic testing results

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 spinal muscular atrophy

Essential facts and insights about Spinal Muscular Atrophy

The ICD-10 code for spinal muscular atrophy includes G12.0 for infantile type and G12.1 for other inherited forms.

Primary ICD-10-CM Codes for spinal muscular atrophy

Infantile spinal muscular atrophy, type I [Werdnig-Hoffmann]
Billable Code

Decision Criteria

clinical Criteria

  • Infantile onset with genetic confirmation

Applicable To

  • Werdnig-Hoffmann disease

Excludes

  • Other inherited spinal muscular atrophy (G12.1)

Clinical Validation Requirements

  • Homozygous SMN1 deletion
  • 1-2 SMN2 copies
  • Absent motor milestones

Code-Specific Risks

  • Incorrect use if genetic testing is not confirmed.

Coding Notes

  • Ensure genetic testing results are documented.

Ancillary Codes

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

Respiratory failure, unspecified

J96.9
Use when documenting respiratory complications in SMA.

Scoliosis, unspecified

M41.9
Use when scoliosis is present in SMA patients.

Differential Codes

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

Other inherited spinal muscular atrophy

G12.1
Late-onset or non-5q SMA with different genetic markers.

Infantile spinal muscular atrophy, type I

G12.0
Infantile onset with specific genetic markers.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Spinal Muscular Atrophy to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code G12.0.

Impact

Clinical: May affect treatment decisions., Regulatory: Increases audit risk., Financial: Potential claim denials.

Mitigation Strategy

Ensure genetic testing is completed and results are documented.

Impact

Reimbursement: May lead to claim denials or reduced reimbursement., Compliance: Increases audit risk., Data Quality: Decreases accuracy of clinical data.

Mitigation Strategy

Ensure genetic testing results are documented and use specific codes.

Impact

High audit risk when using G12.9 without pending genetic test documentation.

Mitigation Strategy

Use specific codes with documented genetic 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 Spinal Muscular Atrophy, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Spinal Muscular Atrophy

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

SMA Type II with respiratory complications

Specialty: Neurology

Required Elements

  • Genetic test results
  • SMN2 copy number
  • Respiratory function assessment

Example Documentation

Patient with SMA Type II (G12.1) confirmed by genetic testing. Requires BiPAP for nocturnal hypoventilation (J96.9).

Examples: Poor vs. Good Documentation

Poor Documentation Example
SMA noted, respiratory issues.
Good Documentation Example
SMA Type II confirmed, SMN1 deletion, 3 SMN2 copies, nocturnal BiPAP required.
Explanation
The good example provides specific genetic and clinical details necessary for accurate coding.

Need help with ICD-10 coding for Spinal Muscular Atrophy? Ask your questions below.

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