G11.0
Congenital nonprogressive ataxia
Hereditary ataxia
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Congenital nonprogressive ataxia
Early-onset cerebellar ataxia
Late-onset cerebellar ataxia
Cerebellar ataxia with defective DNA repair
Hereditary spastic paraplegia
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Leukodystrophy with vanishing white matter disease
Other hereditary ataxias
Hereditary ataxia, unspecified
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None use additional code specified for this code.
These codes cannot be used together with the current code, even if both conditions are present.
None specified for this code.
These codes can be used together with the current code if both conditions are documented.
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