Explore cutting-edge research and innovative approaches in rare disease treatment through this comprehensive conference recording from the Broad Institute's 9th annual Rare Disease Day event. Delve into topics ranging from interventional genetics and orphan drug development to variant interpretation and patient-driven research agendas. Learn from expert speakers as they discuss advancements in areas like Duchenne muscular dystrophy, building rare disease biotech companies, and leveraging population data for improved diagnostics. Gain insights into the challenges and opportunities in rare disease research, including novel genome engineering techniques and strategies for finding undiagnosed patients. This event, featuring collaborations between the Broad Institute and The Termeer Foundation, offers valuable perspectives for researchers, healthcare professionals, and anyone interested in the future of rare disease treatment.