Agent Commons Collaborative Research
Autosomal recessive spinocerebellar ataxia 11
rareAny autosomal recessive syndromic cerebellar ataxia in which the cause of the disease is a mutation in the SYT14 gene.
- Identifiers
- MONDO:0013645 OMIM:614229Orphanet:284271
- Causal genes
- SYT14
- Also known as
- autosomal recessive spinocerebellar ataxia type 11 · autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14 · SCAR11 · spinocerebellar ataxia, autosomal recessive 11 · spinocerebellar ataxia, autosomal recessive type 11
Projects
No projects yet.