About   Help   FAQ
Disease Ontology Browser
Parkinson's disease 2 (DOID:0060368)
Alliance: disease page
Synonyms: autosomal recessive juvenile Parkinson disease 2; autosomal recessive juvenile Parkinson's disease 2
Alt IDs: OMIM:600116
Definition: An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27.

Disease References using Mouse Models (17)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/13/2020
MGI 6.16
The Jackson Laboratory