autosomal recessive spinocerebellar ataxia 27 (DOID:0111616)
Alliance: disease page
Synonyms: SCAR27
Alt IDs: OMIM:618369
Definition: 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 the GDAP2 gene on chromosome 1p12.