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Disease Ontology Browser
autosomal recessive juvenile Parkinson disease 2 (DOID:0060368)
Alt IDs: OMIM:600116, ORDO:2828
Definition: A Parkinson's disease that has_material_basis_in mutation in the parkin gene (PARK2) on chromosome 6q25.2-q27.

Disease References using Mouse Models (14)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory