Autosomal dominant sensory ataxia 1

MONDO:0012166

Any hereditary ataxia in which the cause of the disease is a mutation in the RNF170 gene.

Also known as: ADSA, RNF170 hereditary ataxia, SNAX1, hereditary ataxia caused by mutation in RNF170, Adsa, ataxia, sensory, 1, autosomal dominant

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant sensory ataxia 1 itself.

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