G11.2ICD-10-CM 2027 · Billable
Late-onset cerebellar ataxia
Sibling codes
G11.0– Congenital nonprogressive ataxiaG11.1– Early-onset cerebellar ataxiaG11.3– Cerebellar ataxia with defective DNA repairG11.4– Hereditary spastic paraplegiaG11.5– Hypomyelination - hypogonadotropic hypogonadism - hypodontiaG11.6– Leukodystrophy with vanishing white matter diseaseG11.8– Other hereditary ataxiasG11.9– Hereditary ataxia, unspecified
Inherited from G11: Hereditary ataxia
Excludes2
Part of: G11: Hereditary ataxia