Based at Sanford Research, a not-for-profit research institution, CoRDS is a centralized international patient registry for all rare diseases. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases. The CoRDS registry is free for patients to enroll and for researchers to access. We work with patient advocacy groups, individuals, and researchers to coordinate the advancement of research into the 7,000 rare diseases.

The 5th Annual Sanford Rare Disease Symposium will take place on Friday, February 27th.

Cost is free. Pre-Registration is required.

Sanford Center, Dakota Room
2301 E 60th Street North
Sioux Falls, SD, 57104

Contact or Register here