autosomal dominant Parkinson disease 1
MONDO:0008200Mondo
Findings
No curated finding names autosomal dominant Parkinson disease 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Late onset · Young adult onset
HPO, annotations 2026-09-02
Features
7 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
- 4 of 4 reported patients
- Loss of ambulationHPOHP:0002505
- 4 of 4 reported patients · Late onset
- ParkinsonismHPOHP:0001300
- 4 of 4 reported patients
- RigidityHPOHP:0002063
- 4 of 4 reported patients
- Global brain atrophyHPOHP:0002283
- 2 of 3 reported patients · Late onset
- Resting tremorHPOHP:0002322
- 2 of 4 reported patients
- HallucinationsHPOHP:0000738
- 1 of 3 reported patients
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.
- SNCAHGNC:11138
- Strong · Genomics England PanelApp · Autosomal dominant · 2021
Where it sits
- A kind of
Other names
1 name
Resolves to: autosomal dominant Parkinson disease 1
- Also called
- autosomal dominant Parkinson disease type 1