# juvenile onset Parkinson disease 19A

> Parkinson's disease that has material basis in homozygous mutation in the DNAJC6 gene on chromosome 1p31

**Wikidata**: [Q32136810](https://www.wikidata.org/wiki/Q32136810)  
**Source**: https://4ort.xyz/entity/juvenile-onset-parkinson-disease-19a


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease.
5. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)