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Up to: Congenital nervous system disorder · Autosomal recessive cerebellar ataxia · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Central nervous system malformation
Autosomal recessive spinocerebellar ataxia 20
Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the SNX14 gene.
This condition has no sub-types.