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Disease Ontology Browser
Parkinson's disease 1 (DOID:0060367)
Alliance: disease page
Synonyms: autosomal dominant Parkinson disease 1; autosomal dominant Parkinson's disease 1
Alt IDs: OMIM:168601
Definition: A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1.

Disease References using Mouse Models (54)

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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last database update
07/29/2020
MGI 6.15
The Jackson Laboratory