Parkinson's disease 23

Term ID

DOID:0060896

Synonyms

• autosomal recessive early-onset Parkinson disease 23
• autosomal recessive early-onset Parkinson's disease 23

Definition

An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/26942284

References

• ICD10CM:G20
• MIM:616840

Ontology

Human Disease   ( DOID:0060896 )