For Patients and Families
Genetic diseases impact not only patients but their whole families. These resources will help you understand genetic diseases and the importance of knowing your family health history.
The partnership engages communities on genomics, informs and shares perspectives, and impacts the focus of research.
Find out how learning your family's health history can help you discover your genomic heritage and risks, and guide healthy lifestyle choices.
FAQs about genetic disorders, the impact of genomics on your health, and the emerging science of pharmacogenomics.
A list of genetic, orphan and rare diseases under investigation by researchers at or associated with the National Human Genome Research Institute.
Last updated: December 29, 2018