8A03.1Y Other specified hereditary ataxia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified hereditary ataxia
• Autosomal recessive ataxia
• Autosomal recessive spastic ataxia of Charlevoix-Saguenay
• Ataxia due to Marinesco-Sjögren syndrome
• Autosomal recessive ataxias due to POLG mutations
• Ataxia due to POLG mutations MIRAS
• Autosomal recessive ataxias due to POLG mutations SANDO
• Other autosomal recessive ataxia
• Harding ataxia
• Early onset cerebellar ataxia with retained tendon reflex
• X-linked ataxia
• X-linked intellectual deficit - ataxia - apraxia
• X-linked intellectual deficit, South African type
• X-linked intellectual deficit - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy
• Christianson syndrome
• X-linked spinocerebellar ataxia type 1
• X-linked spinocerebellar ataxia type 3
• X-linked spinocerebellar ataxia type 4
• Fragile X–associated tremor or ataxia syndrome
• Autosomal dominant ataxia
• Autosomal dominant cerebellar ataxia
• Autosomal dominant spastic ataxia
• Dominant ataxia with unknown mutation
• Progressive Ataxia palatal tremor syndrome-GFAP gene mutation

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