Parkinson disease 13, autosomal dominant, susceptibility to
MONDO:0012466Mondo
Findings
No curated finding names Parkinson disease 13, autosomal dominant, susceptibility to yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited susceptibility or predisposition to developing young-onset Parkinson disease, in which the cause of the disease is a mutation in the HTRA2 gene.
Definition from the Mondo Disease Ontology (MONDO:0012466), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- BradykinesiaHPOHP:0002067
- Parkinsonism with favorable response to dopaminergic medicationHPOHP:0002548
- Middle age onset
- RigidityHPOHP:0002063
- TremorHPOHP:0001337
Where it sits
- A kind of
Other names
4 names
Resolves to: Parkinson disease 13, autosomal dominant, susceptibility to
- Also called
- HTRA2 young-onset Parkinson diseasePARK13Parkinson disease 13young-onset Parkinson disease caused by mutation in HTRA2