# autosomal recessive spinocerebellar ataxia 13

> Human disease

**Wikidata**: [Q21124572](https://www.wikidata.org/wiki/Q21124572)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-spinocerebellar-ataxia-13


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)