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Spinocerebellar ataxia, autosomal recessive 24
rareAny autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.
- Identifiers
- MONDO:0014934 OMIM:617133
- Causal genes
- UBA5
- Also known as
- autosomal recessive cerebellar ataxia caused by mutation in UBA5 · SCAR24 · spinocerebellar ataxia, autosomal recessive 24; SCAR24 · spinocerebellar ataxia, autosomal recessive type 24 · UBA5 autosomal recessive cerebellar ataxia
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