G11.3: Cerebellar ataxia with defective DNA repair
G11.3 is a billable, specific ICD-10-CM code for cerebellar ataxia with defective dna repair. It is valid for submission on a claim.
Check G11.3 with the rest of the claim: free scrubberExcludes2: not included here, but may coexist
The excluded condition is not part of this code, but a patient can have both. You may code both.
Inclusion terms
Alternative wordings a physician may use in the chart for this same code.
- Ataxia telangiectasia [Louis-Bar]
Other codes that can never be billed with G11.3
Their own Excludes1 notes name this code, so the conflict is not listed above.
Risk adjustment
G11.3 risk-adjusts. Under the CMS-HCC V28 model it maps to this category:
- HCC 200 Friedreich and Other Hereditary Ataxias; Huntington Disease0.279 RAF
Coefficient shown for the Community Non-dual Aged segment. A higher HCC in the same hierarchy will suppress this one, so capturing it does not always add score. Look up the whole chart to see which of its HCCs the hierarchy would zero.
Medicare coverage
G11.3 is named in 24 Medicare coverage policies: 24 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A52507External Infusion Pumps - Policy Article
- A52509Intravenous Immune Globulin - Policy Article
- A53057Billing and Coding: Home Health Occupational Therapy
- A53064Billing and Coding: Outpatient Occupational Therapy
Alphabetic index entries that lead here
- Ataxia-telangiectasia(Louis-Bar)
- Boder-Sedgwick syndrome(ataxia-telangiectasia)
- Louis-Bar syndrome(ataxia-telangiectasia)
- Ataxia, ataxy, ataxic›telangiectasia(Louis-Bar)
- Syndrome›ataxia-telangiectasia
- Syndrome›Boder-Sedgewick
- Syndrome›Louis-Barré
- Telangiectasia, telangiectasis›ataxic(cerebellar) (Louis-Bar)
- Ataxia, ataxy, ataxic›cerebellar›with defective DNA repair
Code history
Unchanged in every release from FY2024 to FY2027.
Other codes under G11
- G11.0Congenital nonprogressive ataxia
- G11.1Early-onset cerebellar ataxia
- G11.2Late-onset cerebellar ataxia
- G11.4Hereditary spastic paraplegia
- G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6Leukodystrophy with vanishing white matter disease
- G11.8Other hereditary ataxias
- G11.9Hereditary ataxia, unspecified