2026 ICD-10-CM Diagnosis Code G11.2Late-onset cerebellar ataxia
ICD-10-CM Codes›G00–G99›G10-G14›G11
- Billable — Valid for Submission
- Chronic Condition
G11.2 is a billable ICD-10-CM diagnosis code for late-onset cerebellar ataxia. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). The code is restricted by the Medicare Code Editor to adult patients (age 15 through 124). In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other nervous system disorders (often hereditary or degenerative).
Code Identity
Code Classification
Code EditsBilling
Medicare Code Editor checks that affect claim validity for G11.2.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Adult-onset autosomal recessive cerebellar ataxia
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
- Azorean disease
- Azorean disease, type I
- Azorean disease, type II
- Azorean disease, type III
- Azorean disease, type IV
- Episodic ataxia
- Hereditary cerebellar atrophy
- Late onset cerebellar ataxia
- Marie's cerebellar ataxia
- Periodic ataxia
- Progressive cerebellar ataxia
- Progressive cerebellar ataxia with hypogonadism
- Progressive cerebellar ataxia with palatal myoclonus
- Progressive spinocerebellar ataxia with decreased tendon reflexes
- PUM1-related cerebellar ataxia
- Spinocerebellar ataxia type 45
- Spinocerebellar ataxia type 46
- Sporadic adult-onset ataxia of unknown etiology
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Ataxia, ataxy, ataxic - R27.0
- cerebellar (hereditary) - G11.9
- late-onset (Marie's) - G11.2
- Marie's (cerebellar) (heredofamilial) (late- onset) - G11.2
- Sanger-Brown's (hereditary) - G11.2
- Marie's
- cerebellar ataxia (late-onset) - G11.2
- Sanger-Brown ataxia - G11.2
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Ataxia, ataxy, ataxic
- cerebellar (hereditary)
- late-onset (Marie's)
- Ataxia, ataxy, ataxic
- Marie's (cerebellar) (heredofamilial) (late- onset)
- Ataxia, ataxy, ataxic
- Sanger-Brown's (hereditary)
- Marie's
- cerebellar ataxia (late-onset)
- Sanger-Brown ataxia
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Cerebellar Disorders
When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. Problems with the cerebellum include:
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert G11.2 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About G11.2Overview
Is G11.2 (Hereditary ataxia) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report late-onset cerebellar ataxia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
Who can G11.2 be reported for?
The Medicare Code Editor checks late-onset cerebellar ataxia against patient demographics: this code is intended for adult patients (age 15 through 124). Claims outside these limits are flagged as inconsistent.
What is the ICD-9 equivalent of G11.2?
Under the General Equivalence Mappings, late-onset cerebellar ataxia converts to ICD-9-CM 334.2 (primary cerebellar degen). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
