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Disease Ontology Browser
Parkinson's disease 17 (DOID:0060897)
Alliance: disease page
Synonyms: autosomal dominant Parkinson disease 17; 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 (2)
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
12/17/2024
MGI 6.24 		The Jackson Laboratory