"DOID:0111616"^^ . "An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs that has_material_basis_in homozygous or compound heterozygous mutation in GDAP2 on chromosome 1p12."^^ . "SCAR27"@en . "OMIM:618369"^^ . "disease_ontology"^^ . "autosomal recessive spinocerebellar ataxia 27"^^ . . . .