About   Help   FAQ
Disease Ontology Browser
juvenile onset Parkinson disease 19A (DOID:0060891)
Alt IDs: OMIM:615528, ICD10CM:G20, ORDO:391411
Definition: A Parkinson's disease that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
06/13/2017
MGI 6.10
The Jackson Laboratory