Autosomal Recessive Ataxia Due to Pex10 Deficiency, is also known as mild peroxisomal disorder due to pex10 deficiency. An important gene associated with Autosomal Recessive Ataxia Due to Pex10 Deficiency is PEX10 (Peroxisomal Biogenesis Factor 10). Related phenotypes are motor axonal neuropathy and progressive cerebellar ataxia