Educational Content: This article is for informational purposes only and does not constitute medical advice. Always consult a healthcare provider for diagnosis and treatment.
Definition of Familial Parkinson disease type 2
Medically reviewed by Dr. Otari Nergadze, Neurosurgeon | Updated: January 2026
Familial Parkinson disease type 2: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in the gene encoding parkin on chromosome 6q25.2-q27. Also known as PARK2.
