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
RT @RareDiseases: RETWEET. The #raredisease community MUST ACT NOW & urge Senators to #VoteNO. https://t.co/gcp9zvJlD5
RT @Rose_of_Sharon8: Hit 1200 +1500 at @KFS_Freedom today! RARE DISEASE patient impact! @TwitterMoments @GlobalGenes @SanfordCoRDS @RareAdv…
RT @NIHDirector: Mismatch repair defects predict which #cancer patients will benefit from #immunotherapy drug. Learn more! #NIH https://t.c…
Hit 1200 +1500 at @KFS_Freedom today! RARE DISEASE patient impact! @TwitterMoments @GlobalGenes @SanfordCoRDS @RareAdvocates @RareDiseases
RT @RareDiseases: What is a #raredisease? Who is affected in the U.S.? Retweet to raise awareness. https://t.co/Km4DUP3xz7