There are over 6,000 genetic disorders that can be passed down through the generations, many of which are fatal or severely debilitating. Since 1997, the GDF has worked with Mount Sinai to help provide funding for research to improve early detection and treatment options for many of these disorders.
See some of the most notable ways in which GDF and its supporters have made an impact over the past year in advancing our mission to help prevent, manage and treat inherited genetic diseases. View our latest News Brief here. You can sign up to receive regular news and updates from GDF at the top of this page.
The GDF has partnered with the Department of Genetics and Genomic Sciences at Mount Sinai in New York City, one of the largest medical genetics centers in the world. Recognized as a leader in its field, it has more than 50 internationally recognized physician and scientist faculty members and has made numerous contributions to the diagnosis, prevention and treatment of genetic diseases. Learn how advances at Mount Sinai have impacted the lives of thousands of people and provide hope for the future.
Being diagnosed with a genetic disease can be extremely difficult and confusing for you and your family. If you or a loved one has been diagnosed recently, the GDF may be able to help you navigate through this complicated time. Through our affiliation with Mount Sinai’s Department of Genetics and Genomic Sciences, we can help connect you with world-class physicians and genetic counselors in specific disease groups. Learn more on our newly diagnosed patient resource page.
Your support can lead to remarkable gene discoveries and treatments that fight against genetic diseases.
Learn how the GDF has used its fundraising efforts to help further research programs at Mount Sinai.
Gaucher Disease is the most common of the lipid storage diseases. Learn about its symptoms, how it is inherited and available treatments.
The National Organization for Rare Disorders (NORD) is an invaluable resource for people with rare "orphan" diseases. View NORD news and events.
This year’s Miles for Mia Memorial 5K Walk/Run was another big success in support of genetic disease research and education.
Miles for Mia, a benefit dedicated to the life of Mia Jeanette Walts, will be held on Saturday, June 2, 2018 in Brighton, MI.
Acclaimed portrait photographer Karen Haberberg recently turned her lens on families raising children with rare genetic conditions in a stunning new book.