 Hi, my name is Michelle Snyder, and today I will share with you a partnership for educating healthcare providers on rare diseases. The National Human Genome Research Institute, or NHGRI, is one of the 27 institutes and centers that make up the National Institutes of Health. NHGRI is devoted to advancing health through genome research. Healthcare providers receive limited hours of education on genomics. It takes an average of five years to diagnose a child with a rare disease. Improved education of providers can limit time spent in the diagnostic odyssey. NHGRI is working to improve genomic education for healthcare providers and improve patient care. The Inner Society Coordinating Committee for Practitioner Education in Genomics, or ISCCPEG, was founded in 2013 to address these needs. ISCCPEG brings together experts in genetics, in primary care, nursing care, and specialty care to identify educational needs, develop potential solutions, share best practices, and develop resources. There are five ISCCPEG project groups, including rare diseases, pharmacogenomics, direct to consumer genetic testing, inclusive genetics, and obstetrics and gynecology. I lead the Rare Diseases Project Group of ISCCPEG, and our group aims to develop educational resources that address the challenges of rare diseases, such as diagnostic delays, lack of available treatment guidelines, and limited referral pathways. Visit us today at the ISCCPEG virtual booth. You can also join the network of experts at genome.gov. You can view the available resources for healthcare professionals on the genome.gov website under the health section. For more information about ISCCPEG, contact Donna Mezersmith at Donna.Mezersmith at NIH.gov. For more information about the Rare Diseases Project Group, contact me, Michelle Snyder at Michelle.Snyder2 at NIH.gov. Thank you.