# autosomal recessive spinocerebellar ataxia 18

> Human disease

**Wikidata**: [Q21124560](https://www.wikidata.org/wiki/Q21124560)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-spinocerebellar-ataxia-18


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)