GenTIGSA Gene Database on Rare Genetic Disorders
Spinocerebellar Ataxia Type 1  
Disease Aliases (8)

Atxn1 autosomal dominant cerebellar ataxia type i

Autosomal dominant cerebellar ataxia type i caused by mutation in atxn1

Cerebelloparenchymal disorder i

Menzel type opca

Olivopontocerebellar atrophy i

Olivopontocerebellar atrophy iv

Sca1

Schut-haymaker type opca

Associated Genes (0)
 

Cross-references of Spinocerebellar ataxia type 1 OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations