GenTIGSA Gene Database on Rare Genetic Disorders
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Spinocerebellar Ataxia Type 6  
Disease Aliases (11)

Ataxia 6, spinocerebellar

Ataxia 6s, spinocerebellar

Cacna1a autosomal dominant cerebellar ataxia type iii

Sca6

Spinocerebellar ataxia 6s

Spinocerebellar ataxia-6

Spinocerebellar ataxia 6

Spinocerebellar ataxia type 6

Type 6 spinocerebellar ataxia

Autosomal dominant cerebellar ataxia type iii caused by mutation in cacna1a

Spinocerebellar ataxia 6; sca6

Associated Genes (1)
 

NCBI-RefSeq:  CACNA1A   (Calcium voltage-gated channel subunit alpha1 A)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Spinocerebellar ataxia type 6 OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations