February 23, 2016
CoRDS is launching a new international rare disease registry with Kabuki Syndrome Network this Rare Disease Day! The Coordination of Rare Diseases at Sanford (CoRDS) registry 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. Learn more about Kabuki Syndrome and watch for updates regarding the registry by visiting the Kabuki Syndrome Network.