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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; Parkinson disease juvenile type 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 (18)
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)
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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory