Category: G11 - Hereditary ataxia

 Chapter Notes

 G11

Hereditary ataxia

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]

Cockayne's syndrome (Q87.19)

other disorders of purine and pyrimidine metabolism (E79.-)

xeroderma pigmentosum (Q82.1)

 G11.4

Hereditary spastic paraplegia

 G11.8

Other hereditary ataxias

 G11.9

Hereditary ataxia, unspecified

Hereditary cerebellar ataxia NOS

Hereditary cerebellar degeneration

Hereditary cerebellar disease

Hereditary cerebellar syndrome