parkinsonism due to ATP13A2 deficiency
ORPHA: 314632
Overview
human disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with parkinsonism due to ATP13A2 deficiency, sourced from HPO and Orphanet clinical annotations.
RigidityDystoniaMyoclonusTremorBradykinesiaPostural instabilityDiffuse cerebral atrophyParkinsonism with favorable response to dopaminergic medicationBabinski signUpgaze palsyCognitive impairmentDysarthriaGait disturbanceMuscle weaknessAbnormal caudate nucleus morphologyFatigueDepressionPostural tremor
Classification & Codes
Orphanet Code
ORPHA:314632parkinsonism due to ATP13A2 deficiency
| Orphanet | ORPHA:314632 |
| Treatments | 0 drug(s) |
| Symptoms on record | 18 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO