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Autosomal recessive spinocerebellar ataxia 16
rareAny autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the STUB1 gene.
- Identifiers
- MONDO:0014339 OMIM:615768Orphanet:412057
- Causal genes
- STUB1
- Also known as
- autosomal recessive cerebellar ataxia caused by mutation in STUB1 · autosomal recessive spinocerebellar ataxia type 16 · SCAR16 · spinocerebellar ataxia autosomal recessive type 16 · spinocerebellar ataxia, autosomal recessive 16
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