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Autosomal recessive spinocerebellar ataxia 17
rareAny autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.
- Identifiers
- MONDO:0014503 OMIM:616127Orphanet:453521
- Causal genes
- CWF19L1
- Also known as
- autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1 · autosomal recessive spinocerebellar ataxia type 17 · CWF19L1 autosomal recessive congenital cerebellar ataxia · SCAR17 · spinocerebellar ataxia autosomal recessive type 17
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