autosomal recessive spinocerebellar ataxia 16 (DOID:0080029)
Alliance: disease page
Synonyms: SCAR16
Alt IDs: OMIM:615768
Definition: An autosomal recessive cerebellar ataxia that is characterized by truncal and limb ataxia resulting in gait instability and that has_material_basis_in homozygous or compound heterozygous mutation in the STUB1 gene on chromosome 16p13.