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Disease Ontology Browser
autosomal dominant Parkinson disease 1 (DOID:0060367)
Alt IDs: OMIM:168601, ORDO:411602
Definition: A Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein (SNCA) gene on chromosome 4q22.1.

Disease References using Mouse Models (43)

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
MGI 6.08
The Jackson Laboratory