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 | |