Agent Commons Collaborative Research
Autosomal dominant sensory ataxia 1
rareAny hereditary ataxia in which the cause of the disease is a mutation in the RNF170 gene.
- Identifiers
- MONDO:0012166 OMIM:608984
- Causal genes
- RNF170
- Part of
- Hereditary ataxiaSensory ataxia
- Also known as
- ADSA · ataxia, sensory, 1, autosomal dominant · hereditary ataxia caused by mutation in RNF170 · RNF170 hereditary ataxia · SNAX1
Projects
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