/spinocerebellar ataxia, autosomal recessive 29

spinocerebellar ataxia, autosomal recessive 29

Rare Disease

MONDO:0030312

Also Known As

Barakat-Van Ham-Kaya syndromeSCAR29neurodevelopmental disorder with hypotonia and cerebellar ataxiaspinocerebellar ataxia, autosomal recessive 29

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

Charlevoix-Saguenay spastic ataxia

MONDO:0010041

infantile-onset autosomal recessive nonprogressive cerebellar ataxia

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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