The RARE-X KDM5C Data Collection Program allows researchers from around the world to access standardized and deidentified patient data to accelerate research and target therapeutic treatments to improve the lives of patients affected by KDM5C genetic variants. Leveraging the RARE-X platform in conjunction with other rare disease communities can increase the likelihood that KDM5C will be included in cross-disease research. There is no cost to our community to participate!

This Launch Party session goes over the basics of how to enroll!