# young-onset Parkinson disease

> human disease

**Wikidata**: [Q32136833](https://www.wikidata.org/wiki/Q32136833)  
**Source**: https://4ort.xyz/entity/young-onset-parkinson-disease


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
4. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000116288/Orphanet_2828)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000116675/Orphanet_2828)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000158828/Orphanet_2828)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000185345/Orphanet_2828)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000188906/Orphanet_2828)
10. [Identifiers.org](https://registry.identifiers.org/registry/doid)
11. UMLS 2023