| G10 |
Huntington's disease |
Notes ↗
|
| G11.0 |
Congenital nonprogressive ataxia |
Notes ↗
|
| G11.10 |
Early-onset cerebellar ataxia, unspecified |
Notes ↗
|
| G11.11 |
Friedreich ataxia |
Notes ↗
|
| G11.19 |
Other early-onset cerebellar ataxia |
Notes ↗
|
| G11.2 |
Late-onset cerebellar ataxia |
Notes ↗
|
| G11.3 |
Cerebellar ataxia with defective DNA repair |
Notes ↗
|
| G11.4 |
Hereditary spastic paraplegia |
Notes ↗
|
| G11.5 |
Hypomyelination - hypogonadotropic hypogonadism - hypodontia |
Notes ↗
|
| G11.6 |
Leukodystrophy with vanishing white matter disease |
Notes ↗
|
| G11.8 |
Other hereditary ataxias |
Notes ↗
|
| G11.9 |
Hereditary ataxia, unspecified |
Notes ↗
|
| G31.80 |
Leukodystrophy, unspecified |
Notes ↗
|
| G90.B |
LMNB1-related autosomal dominant leukodystrophy |
Notes ↗
|
| G93.42 |
Megalencephalic leukoencephalopathy with subcortical cysts |
Notes ↗
|
| G93.43 |
Leukoencephalopathy with calcifications and cysts |
Notes ↗
|
| G93.44 |
Adult-onset leukodystrophy with axonal spheroids |
Notes ↗
|