has material basis in germline mutation in STUB1 autosomal recessive spinocerebellar ataxia 16 autosomal recessive spinocerebellar ataxia type 16 UMLS:C5190574 MEDGEN:1674542 OMIM:615768 GARD:0017689 DOID:0080029 autosomal recessive cerebellar ataxia due to STUB1 deficiency autosomal recessive spinocerebellar ataxia 16 spinocerebellar ataxia autosomal recessive type 16 MONDO:0014339 SCAR16 spinocerebellar ataxia, autosomal recessive type 16 Orphanet:412057 spinocerebellar ataxia, autosomal recessive 16 Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the STUB1 gene. autosomal recessive cerebellar ataxia caused by mutation in STUB1 STUB1 autosomal recessive cerebellar ataxia autosomal recessive cerebellar ataxia