Genetic Disease Foundation Inc

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The Genetic Disease Foundation (GDF) is a non-profit 501c(3) organization established in 1997 by patients and families affected by genetic disorders. The Foundation’s mission is to support research, education and the prevention of genetic diseases.

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136151644

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Parsippany

Address: 389 Interpace Pkwy Ste 3, ParsippanyWeb: Sign in to see organisation websiteICO: 136151644

Genetic Disease Foundation | Jewish Genetic Disease Consortium Genetic Disease Foundation GDF was a founding member of the Jewish Genetic Disease Consortium JGDC whose mission is to educate medical professionals clergy and the general public to increase awareness about genetic diseases and encourage timely and appropriate carrier screening for anyone starting or expending their family. Over its 25year history the GDF raised millions of dollars to help enable advancements in identifying the genetic basis of many diseases and to help raise awarenessaboutcarrier testing and newborn screening as well as increase physician and public awareness of genetic disorders. Funds raised by the Foundation helped enable the purchase of stateoftheart DNA sequencing mass spectrometry and gene mutation detection equipment for Mount Sinais Department of Genetics and Genomic Sciences. This technology helped expedite diagnosis and research for a range of genetic diseases and supported a number of important breakthroughs including In 2007 the GDF provided an endowment to support the creation of the Francis Crick Professorship of Human Genetics at The Icahn School of Medicine at Mount Sinai which was awarded to GDF Medical and Scientific Advisory Board memberDr.

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Matthew

So proud to support the Genetic Disease Foundation and their incredible work in advancing research and awareness for genetic disorders! Together, we can make a difference! 💙🧬

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Sharon

Kudos to the GDF for their dedication to educating and empowering families about genetic diseases. Your efforts are changing lives and providing hope for many! 🙌✨

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Laura

2. What strategies can be implemented to increase funding and support for research on rare genetic disorders and their therapies within the community?

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Patrick

1. How can NGOs effectively collaborate with medical institutions to enhance public education and awareness about genetic diseases and carrier screening?

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