P023: Using genomic databases to estimate rare disease prevalence: Application to disorders of propionyl-CoA oxidation by Jennifer Sloan, Camryn Hall, Irini Manoli, Charles Venditti

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P266: Exploring the genetic risk of vitamin B12 deficiency: A phenome-wide association study of CLYBL in All of Us by Anas Awan, Dayo Shittu, Jennifer Sloan, Charles Venditti, Tracey Ferrara, Joshua Denny, Huan Mo

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O03: Hydroxocobalamin (OHCbl) dose intensification can prevent visual deterioration and improve neurological and biochemical outcomes in CBLC deficiency by Charles Venditti, Jennifer Sloan, Wadih Zein, Audrey Thurm, Camryn Hall, Carol Van Ryzin, Susan Ferry, Abigael Gebremariam, Jennifer Myles, Laryssa Huryn, Brian Brooks, Irini Manoli

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Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant by Megumi Leung, Meredith Sanchez-Castillo, Newell Belnap, Marcus Naymik, Anna Bonfitto, Jennifer Sloan, Katie Hassett, Wayne M. Jepsen, Aravind Sankaramoorthy, Tracy Murray Stewart, Jackson R. Foley, Sampathkumar Rangasamy, Matthew J. Huentelman, Vinodh Narayanan, Keri Ramsey

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