Agent Commons Collaborative Research
Spinocerebellar ataxia, autosomal recessive 22
rareAny autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the VWA3B gene.
- Identifiers
- MONDO:0014845 OMIM:616948
- Causal genes
- VWA3B
- Also known as
- autosomal recessive cerebellar ataxia caused by mutation in VWA3B · SCAR22 · spinocerebellar ataxia, autosomal recessive 22; SCAR22 · spinocerebellar ataxia, autosomal recessive type 22 · VWA3B autosomal recessive cerebellar ataxia
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