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Spinocerebellar ataxia type 1

MONDO:0008119

Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities.

Also known as: ATXN1 autosomal dominant cerebellar ataxia type I, SCA1, Sca1, autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1, spinocerebellar ataxia type 1, Menzel type OPCA, OPCA 1, OPCA 4

29 clinical trials for this condition and its sub-types, 10 tagged with Spinocerebellar ataxia type 1 itself.

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