Solving Medical Mysteries at the Stanford Center for Undiagnosed Diseases

This course aims to educate learners on the process of solving medical mysteries for patients with undiagnosed diseases. The learning outcomes include understanding the role of expert clinicians and cutting-edge diagnostic testing in diagnosing rare diseases, genetic variations, and phenotypes. The course covers topics such as genetic testing, omics technologies, data sharing networks, and therapeutic approaches. The teaching method involves lectures by Stanford Medicine physicians, including real patient stories and case studies. The intended audience for this course includes healthcare professionals, medical students, researchers, and individuals interested in rare diseases and diagnostic medicine.