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G11.3 Cerebellar ataxia with defective DNA repair
BackG11Hereditary ataxiaCategory9 →G11.0Congenital nonprogressive ataxiaCategoryG11.1Early-onset cerebellar ataxiaCategory3 →G11.10Early-onset cerebellar ataxia, unspecifiedCategoryG11.11Friedreich ataxiaCategoryG11.19Other early-onset cerebellar ataxiaCategoryG11.2Late-onset cerebellar ataxiaCategoryG11.3Cerebellar ataxia with defective DNA repairCategoryG11.4Hereditary spastic paraplegiaCategoryG11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontiaCategoryG11.6Leukodystrophy with vanishing white matter diseaseCategoryG11.8Other hereditary ataxiasCategoryG11.9Hereditary ataxia, unspecifiedCategory
CategoryCODABLE
G11.3
Cerebellar ataxia with defective DNA repair
EXAMPLES
Ataxia telangiectasia [Louis-Bar]
EXCLUDES
Excludes2: Cockayne's syndrome (Q87.19)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
- Chapter
- VI · Diseases of the nervous system
- Section
- G10-G14
- Valid from
Source
CMS ICD-10-CM Tabular List, edition FY2026.