 G11 |
 |
Hereditary ataxia  |
| |
| Excludes2 |
cerebral palsy (G80.-)
hereditary and idiopathic neuropathy (G60.-)
metabolic disorders (E70-E88)
|
|
| |
 G11.0 |
|
Congenital nonprogressive ataxia |
|
| |
| G11.1 |
|
Early-onset cerebellar ataxia |
| |
| G11.10 |
|
Early-onset cerebellar ataxia, unspecified |
| | |
| G11.11 |
|
Friedreich ataxia |
| |
| Autosomal recessive Friedreich ataxia | | Friedreich ataxia with retained reflexes |
|
| | |
| G11.19 |
|
Other early-onset cerebellar ataxia |
| |
| Early-onset cerebellar ataxia with essential tremor | | Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia] | | Early-onset cerebellar ataxia with retained tendon reflexes | | X-linked recessive spinocerebellar ataxia |
|
| |
| |
| G11.2 |
|
Late-onset cerebellar ataxia |
| |
|
|
| |
| G11.3 |
|
Cerebellar ataxia with defective DNA repair |
| |
| Ataxia telangiectasia [Louis-Bar] |
| Excludes2 |
Cockayne's syndrome (Q87.19)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
|
|
|
| |
| G11.4 |
|
Hereditary spastic paraplegia |
|
| |
| G11.5 |
|
Hypomyelination - hypogonadotropic hypogonadism - hypodontia |
| |
| 4H syndrome | | Pol III-related leukodystrophy |
|
|
| |
| G11.6 |
|
Leukodystrophy with vanishing white matter disease |
|
| |
| G11.8 |
|
Other hereditary ataxias |
|
| |
| G11.9 |
|
Hereditary ataxia, unspecified |
| |
| Hereditary cerebellar ataxia NOS | | Hereditary cerebellar degeneration | | Hereditary cerebellar disease | | Hereditary cerebellar syndrome |
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