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Disease Ontology Browser
Parkinson disease 17 (DOID:0060897)
Synonyms: autosomal dominant Parkinson disease 17
Alt IDs: OMIM:614203
Definition: A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.

Disease References using Mouse Models (1)

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
06/20/2017
MGI 6.10
The Jackson Laboratory