# Kufor-Rakeb syndrome

> Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment

**Wikidata**: [Q6441908](https://www.wikidata.org/wiki/Q6441908)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Kufor–Rakeb_syndrome)  
**Source**: https://4ort.xyz/entity/kufor-rakeb-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000159363/MONDO_0011706)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)