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.