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G11
Hereditary ataxia
Type 2 Excludes
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Children (12)
Code | Description | Billable | Details |
|---|---|---|---|
| G11.0 | Congenital nonprogressive ataxia | ||
| G11.1 | Early-onset cerebellar ataxia | ||
| G11.10 | Early-onset cerebellar ataxia, unspecified | ||
| G11.11 | Friedreich ataxia | ||
| G11.19 | Other early-onset cerebellar ataxia | ||
| G11.2 | Late-onset cerebellar ataxia | ||
| G11.3 | Cerebellar ataxia with defective DNA repair | Type 2 Excludes (3) | |
| G11.4 | Hereditary spastic paraplegia | ||
| G11.5 | Hypomyelination - hypogonadotropic hypogonadism - hypodontia | ||
| G11.6 | Leukodystrophy with vanishing white matter disease |
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