"2015-10-07T14:55:44Z"^^ . "DOID:0080066"^^ . "lschriml"^^ . . "autosomal recessive spinocerebellar ataxia 20"^^ . "OMIM:616354"^^ . "An autosomal recessive cerebellar ataxia that is characterized by severely delayed psychomotor development with poor or absent speech, wide-based or absent gait, coarse facies, and cerebellar atrophy and that has_material_basis_in homozygous mutation in the SNX14 gene on chromosome 6q14."^^ . . "disease_ontology"^^ . .