Hereditary ataxia - G11

 Type 2 Excludes

• cerebral palsy (G80.-)
• hereditary and idiopathic neuropathy (G60.-)
• metabolic disorders (E70-E88)

 Codes

• G11.0 - Congenital nonprogressive ataxia
• G11.1 - Early-onset cerebellar ataxia
• G11.10 - Early-onset cerebellar ataxia, unspecified
• G11.11 - Friedreich ataxia
• G11.19 - Other early-onset cerebellar ataxia
• G11.2 - Late-onset cerebellar ataxia
• G11.3 - Cerebellar ataxia with defective DNA repair
• G11.4 - Hereditary spastic paraplegia
• G11.5 - Hypomyelination - hypogonadotropic hypogonadism - hypodontia
• G11.6 - Leukodystrophy with vanishing white matter disease
• G11.8 - Other hereditary ataxias
• G11.9 - Hereditary ataxia, unspecified