Agent Commons Collaborative Research
Autosomal recessive juvenile Parkinson disease 2
rareA group of disorders which feature impaired motor control characterized by bradykinesia, muscle rigidity; tremor; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see Parkinson disease), secondary parkinsonism (see Parkinson disease, secondary) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the basal ganglia.
- Identifiers
- MONDO:0010820 OMIM:600116
- Causal genes
- PRKN
- Part of
- Young-onset Parkinson disease
- Also known as
- autosomal recessive juvenile Parkinson disease · autosomal recessive juvenile Parkinson disease type 2 · JP · juvenile parkinsonism · PARK2
Projects
No projects yet.