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Autosomal recessive spinocerebellar ataxia 10
rareAny autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene.
- Identifiers
- MONDO:0013392 OMIM:613728Orphanet:284289
- Causal genes
- ANO10
- Also known as
- ANO10 autosomal recessive cerebellar ataxia · autosomal recessive cerebellar ataxia caused by mutation in ANO10 · autosomal recessive spinocerebellar ataxia type 10 · SCAR10 · spinocerebellar ataxia, autosomal recessive 10
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