Establishes State Parkinson's disease registry.

This bill establishes a statewide Parkinson's disease registry in New Jersey to track cases and gather health data. Healthcare providers must report diagnosed cases (including past diagnoses) to the Department of Health, with patients able to opt out at any time. Data collected includes diagnosis, treatment, and optional demographic details like age or race, but all information is kept confidential using coded identifiers. The registry aims to support research and public health efforts by sharing de-identified data with approved researchers, other states, or health agencies, while strictly protecting patient privacy.