Category: G11 - Hereditary ataxia
Chapter Notes
Hereditary ataxia
cerebral palsy (G80.-)
hereditary and idiopathic neuropathy (G60.-)
metabolic disorders (E70-E88)
Congenital nonprogressive ataxia
Early-onset cerebellar ataxia
Early-onset cerebellar ataxia, unspecified
Friedreich ataxia
Autosomal recessive Friedreich ataxia
Friedreich ataxia with retained reflexes
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
Late-onset cerebellar ataxia
Cerebellar ataxia with defective DNA repair
Ataxia telangiectasia [Louis-Bar]
Cockayne's syndrome (Q87.19)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
Hereditary spastic paraplegia
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
4H syndrome
Pol III-related leukodystrophy
Leukodystrophy with vanishing white matter disease
Other hereditary ataxias
Hereditary ataxia, unspecified
Hereditary cerebellar ataxia NOS
Hereditary cerebellar degeneration
Hereditary cerebellar disease
Hereditary cerebellar syndrome
