Developed by the National Coordinating Center for the Regional Genetics Networks (NCC), the Genetics Policy Hub provides resources related to genetics policy across the U.S. Within the hub, you can find the latest legislation and regulation at the state and federal level, latest information on Medicaid coverage policy, information about specific policy topics and related …
The Direct-to-Consumer Genetic Testing (DTC-GT) Frequently Asked Questions (FAQ) resource designed for the general clinician who may see patients requesting guidance on DTC-GT. This FAQ is intended to help healthcare professionals understand the diverse landscape of DTC-GT, the benefits and limitations of these tests and how results of DTC-GT may affect their patients’ health, wellness …
The NORD Rare Disease Video Library houses educational videos on rare diseases for patients, caregivers, students, professionals and the public. NORD works with medical experts and patient organizations to develop the videos, which are made possible by individual donations, educational grants and corporate sponsorship.
The Genetic Testing Registry (GTR®) provides a central location for voluntary submission of genetic test information by providers.
GARD is a program of the National Center for Advancing Translational Sciences (NCATS) to provide access to current, reliable, and easy to understand information about rare or genetic diseases in English or Spanish.
Defines uniform and internationally accepted terms to describe the human phenotype for the craniofacies in general, the major components of the face, and the hands and feet.
Clinical Trials is a database of privately and publicly funded clinical trials conducted around the world.
The purpose of this website is to provide a tool that is helpful for the clinician in diagnosing syndromic disorders across varied populations.
The ACMG ACT Sheets and their accompanying algorithms are great resources for health care providers looking for information on genetic conditions (identified through newborn screening and beyond) to help inform clinical decision making.
The purpose of NORD Online Physician Guides is to provide a resource for clinicians about specific rare disorders to facilitate the timely diagnosis and treatment of their patients. Family physicians, pediatricians, and other primary care providers play an important role in early identification and long-term management of patients with rare diseases. It is important for …