Centers of Excellence - National Organization for Rare Disorders NORD is committed to breaking down silos and building bridges so that people living with a rare disease can achieve their best health and well-being Our belief is that the NORD Rare Disease Centers of Excellence program is the next big stride forward for rare disease patients and care, to improve health equity and create critical new connections to resources and specialists across our nation
List of Rare Diseases | A-Z Database | NORD What Is the NORD ® Rare Disease Database? The NORD Rare Disease Database is an inclusive and comprehensive list of rare diseases based on information from established rare disease ontologies and it is an ongoing project made possible by a close collaboration with MONDO, Orphanet, and Online Mendelian Inheritance in Man (OMIM)
Rare Diseases Support, Resources Help | NORD Can NORD help find a medical expert for my rare disease? Many patient organizations provide lists of medical experts Search NORD’s Organizational Database to find disease-specific patient advocacy organizations NORD Rare Disease Centers of Excellence are diagnosing and treating thousands of rare disease patients
Rare Disease Day - Faces of Rare | NORD Faces of Rare: Join our online community wall campaign Share your story, connect with others facing rare challenges Unite for awareness!
How NORD Can Help - Resources, Financial Support, More | NORD Help with Rare Disease Whether you need help getting a diagnosis, finding resources to assist in finding a specialist, finding a clinical trial, paying medical bills, or affording drugs, NORD is here We provide resources, rare disease information, and ways to get involved With our network of members, advocates, and partners, we make critical connections and work to make an impact for every
Rare Disease Day - Rare Disease Day Events | NORD Join NORD on Rare Disease Day! Discover impactful sessions, engaging speakers, and community events Raise awareness, foster connections, and make a difference Be a part of the rare disease community’s journey