autosomal dominant Parkinson disease 8
MONDO:0011764Mondo
Findings
No curated finding names autosomal dominant Parkinson disease 8 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 LRRK2 gene.
Definition from the Mondo Disease Ontology (MONDO:0011764), read 2026-09-29. CC BY 4.0.
- Onset and course
- Late 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.
- LRRK2HGNC:18618
- Definitive · Laboratory for Molecular Medicine · Autosomal dominant · 2020
- Strong · Genomics England PanelApp · Autosomal dominant · 2021
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
4 names
Resolves to: autosomal dominant Parkinson disease 8
- Also called
- autosomal dominant Parkinson disease type 8LRRK2 Parkinson diseaseParkinson disease 8Parkinson disease caused by mutation in LRRK2