ICD-10-CM › G00-G99 › G10-G14 › G11 Hereditary ataxia › G11.1
G11.1
Early-onset cerebellar ataxia
Not billableICD-10-CM diagnosis code.
This code exists but cannot be submitted on its own. It groups the more specific codes beneath it.
Submit one of these 3 more specific codes instead:
What has happened to this code
Every change the publisher made, from 2007 to now. Entries marked draft are from the pre-implementation releases: ICD-10 took effect on 1 October 2015, so nothing before FY2016 was ever valid on a claim.
- FY2007 Added to the draft code set draft Early-onset cerebellar ataxia
- FY2021 Stopped being billable
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from G11 Hereditary ataxia
Excludes2 - not included here
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Codes in the same group
| Code | Description | Status |
|---|---|---|
| G11.0 | Congenital nonprogressive ataxia | Valid |
| G11.2 | Late-onset cerebellar ataxia | Valid |
| G11.3 | Cerebellar ataxia with defective DNA repair | Valid |
| G11.4 | Hereditary spastic paraplegia | Valid |
| G11.5 | Hypomyelination - hypogonadotropic hypogonadism - hypodontia | Valid |
| G11.6 | Leukodystrophy with vanishing white matter disease | Valid |
| G11.8 | Other hereditary ataxias | Valid |
| G11.9 | Hereditary ataxia, unspecified | Valid |