# autosomal recessive spinocerebellar ataxia 12

> human disease

**Wikidata**: [Q21124570](https://www.wikidata.org/wiki/Q21124570)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-spinocerebellar-ataxia-12


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000186153/MONDO_0013687)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)