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Disease Ontology Browser
Parkinson's disease 15 (DOID:0060372)
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Synonyms: autosomal recessive early-onset Parkinson disease 15; autosomal recessive early-onset Parkinson's disease 15; pallidopyramidal syndrome; Parkinsonian-pyramidal syndrome
Alt IDs: OMIM:260300
Definition: An early-onset Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3.


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
11/10/2020
MGI 6.16
The Jackson Laboratory