Welcome to the Coordination of Rare Diseases at Sanford (CoRDS)!
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.
How does enrollment in the CoRDS Registry work?
Twitter Updates on Sanford CoRDS
Calling all South Dakota natives in the #raredisease community - @RareAdvocates has travel stipends left for their… https://t.co/do9RywBwMi
RT @SanfordHealth: The inaugural winners of the Sanford Lorraine Cross Award are Drs. Jean Bennett and Katherine High. #innovation #genomic…
RT @nature: The Galapagos Islands tortoise named Lonesome George was the last member of his species when he died in 2012. His genome sequen…