Parkinson disease 17
MONDO:0013625Mondo
Findings
No curated finding names Parkinson disease 17 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Parkinson disease in which the cause of the disease is a mutation in the VPS35 gene.
Definition from the Mondo Disease Ontology (MONDO:0013625), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- VPS35HGNC:13487
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · Genomics England PanelApp · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2018
Where it sits
- A kind of
Other names
3 names
Resolves to: Parkinson disease 17
- Also called
- Parkinson disease caused by mutation in VPS35Parkinson disease type 17VPS35 Parkinson disease