About   Help   FAQ
Disease Ontology Browser
Parkinson's disease 23 (DOID:0060896)
Alliance: disease page
Synonyms: autosomal recessive early-onset Parkinson disease 23; autosomal recessive early-onset Parkinson's disease 23
Alt IDs: OMIM:616840, ICD10CM:G20
Definition: An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory