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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)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory