Reference: 38 CFR 4.124a, DC 8017

What is the VA rating for Amyotrophic Lateral Sclerosis?

The published Amyotrophic Lateral Sclerosis schedule uses specific diagnostic codes.

Condition Overview & Clinical Scope

Under 38 CFR 4.124a, Diagnostic Code 8017, Amyotrophic Lateral Sclerosis (ALS) is rated at 100 percent.

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Common Questions & FAQs

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What are you trying to understand about amyotrophic lateral sclerosis?

Overview

About this condition

Under 38 CFR 4.124a, Diagnostic Code 8017, Amyotrophic Lateral Sclerosis (ALS) is rated at 100 percent.

Regulatory authority: 38 CFR 4.124a, DC 8017

This guide is educational only. RatingScope does not diagnose ALS, cannot determine service connection, and does not predict a VA decision. This provides the standard regulatory rule for ALS severity.

Percentage Guides

Understanding Your Percentage

Select a pathway to see what the published criteria ask about, what records may clarify it, and what should not be assumed.

100%

Highest listed pathway

Standard rating for ALS.

Review CFR criteria, examples, and evidence
Official CFR language
8017 Amyotrophic lateral sclerosis: 100
What the published criteria say
ALS receives a 100 percent rating.
Medical evidence
Confirmed diagnosis of Amyotrophic Lateral Sclerosis

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Understand the details behind the criteria

Use these short guides to connect published terms with the records and observations that may clarify them.

Statutory total disability designation and progressive complications

Diagnostic Code 8017 lists a 100 percent schedular evaluation for amyotrophic lateral sclerosis (ALS).

  • This describes the percentage specified by the rating schedule for ALS; a VA benefits determination separately depends on the requirements applicable to the individual claim.
  • Special Monthly Compensation (SMC) may apply when the disease results in loss of use of extremities, need for regular aid and attendance, or respiratory failure.
  • Clinical care focuses on multidisciplinary management of motor weakness, bulbar symptoms (speech and swallowing), and ventilatory support.

Records to review: Neurology consultation reports confirming definitive ALS diagnosis based on clinical and electrodiagnostic criteria; EMG and nerve conduction studies showing widespread active denervation and reinnervation; Pulmonary function and speech-language pathology assessments.

Evidence

Evidence that may clarify the published criteria

Medical Evidence 1

A confirmed medical diagnosis of Amyotrophic Lateral Sclerosis (ALS).

A diagnosis alone does not identify which percentage pathway applies.

VA forms and DBQs (from VA.gov)

Downloadable DBQs & Supporting Claim Forms

The public DBQ shows the kinds of findings an examiner may record. A veteran may review it, or may share it with a private clinician, before a C&P exam. RatingScope does not tell any person what to submit.

Terminology

Plain-English terms

Common Questions

Questions veterans commonly ask

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Amyotrophic Lateral Sclerosis (ALS) is evaluated under the Neurological Diseases assessment

RatingScope compares Amyotrophic Lateral Sclerosis (ALS) records using the published criteria in the Neurological Diseases assessment. Compare your documented records against the criteria.

Informational guidance only. RatingScope does not predict, decide, or guarantee VA outcomes.

Compare records in the Neurological Diseases assessment

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Secondary conditions

Conditions commonly connected to Amyotrophic Lateral Sclerosis

No commonly documented secondary connections are tracked for Amyotrophic Lateral Sclerosis yet.

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VA Math & Combined Ratings

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Evidence Center

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