# spinocerebellar ataxia type 13

> Human disease

**Wikidata**: [Q2310947](https://www.wikidata.org/wiki/Q2310947)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Spinocerebellar_ataxia_type-13)  
**Source**: https://4ort.xyz/entity/spinocerebellar-ataxia-type-13


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000131398/MONDO_0011529)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)