G11.8
G11.8: Other hereditary ataxias
Billable / specific codeICD-10-CM
G11.8 is a billable, specific ICD-10-CM code for other hereditary ataxias. It is valid for submission on a claim.
Check G11.8 with the rest of the claim: free scrubberOther codes that can never be billed with G11.8
Their own Excludes1 notes name this code, so the conflict is not listed above.
Risk adjustment
G11.8 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
G11.8 is named in 14 Medicare coverage policies: 14 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A53057Billing and Coding: Home Health Occupational Therapy
- A53064Billing and Coding: Outpatient Occupational Therapy
- A53065Billing and Coding: Outpatient Physical Therapy
- A54969Billing and Coding: Nerve Conduction Studies and Electromyography
Alphabetic index entries that lead here
- Ataxia, ataxy, ataxic›hereditary›specified NEC
- Disease, diseased›spinocerebellar›specified NEC
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
- G11.3Cerebellar ataxia with defective DNA repair
- G11.4Hereditary spastic paraplegia
- G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6Leukodystrophy with vanishing white matter disease
- G11.9Hereditary ataxia, unspecified