autosomal recessive early-onset Parkinson disease 6
MONDO:0011613Mondo
Findings
No curated finding names autosomal recessive early-onset Parkinson disease 6 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 PINK1 gene.
Definition from the Mondo Disease Ontology (MONDO:0011613), read 2026-09-29. CC BY 4.0.
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.
- PINK1HGNC:14581
- Definitive · Ambry Genetics · Autosomal recessive · 2018
- Strong · Genomics England PanelApp · Autosomal recessive · 2021
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Limited · Ambry Genetics · Autosomal dominant · 2024
Where it sits
- A kind of
Other names
2 names
Resolves to: autosomal recessive early-onset Parkinson disease 6
- Also called
- Parkinson disease caused by mutation in PINK1PINK1 Parkinson disease