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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

• Early-onset cerebellar ataxia with essential tremor
• Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia]
• Early-onset cerebellar ataxia with retained tendon reflexes
• Friedreich's ataxia (autosomal recessive)
• X-linked recessive spinocerebellar ataxia

G11.2

Late-onset cerebellar ataxia

G11.3

Cerebellar ataxia with defective DNA repair

• Cockayne's syndrome (Q87.1)
• other disorders of purine and pyrimidine metabolism (E79.-)
• xeroderma pigmentosum (Q82.1)

• Ataxia telangiectasia [Louis-Bar]

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