Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.
Comprehensive, easy-to-understand information about this condition
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Charlevoix-Saguenay spastic ataxia
MONDO:0010041
infantile-onset autosomal recessive nonprogressive cerebellar ataxia
MONDO:0011950
autosomal recessive spinocerebellar ataxia 7
MONDO:0012235
autosomal recessive ataxia, Beauce type
MONDO:0012549
RIDDLE syndrome
MONDO:0012764
autosomal recessive ataxia due to ubiquinone deficiency
MONDO:0012784