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Disease Ontology Browser
Parkinson's disease 25 (DOID:0070486)
Alliance: disease page
Synonyms: autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development; PARK25
Alt IDs: OMIM:620482
Definition: An early-onset Parkinson's disease characterized by mild to moderately impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the PTPA gene on chromosome 9q34.11.

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
11/19/2024
MGI 6.24 		The Jackson Laboratory