# spinocerebellar ataxia type 40

> Human disease

**Wikidata**: [Q21097781](https://www.wikidata.org/wiki/Q21097781)  
**Source**: https://4ort.xyz/entity/spinocerebellar-ataxia-type-40


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)