Genetic and Rare Diseases (GARD) Information Center
GARD offers free access to reliable information for individuals and families affected by rare diseases.
Genetic and Rare Diseases Information Center
The Genetic and Rare Diseases (GARD) Information Center information specialists are available to answer questions and provide support through phone and email. GARD uses information from reputable sources, such as the National Library of Medicine, Orphanet, Human Phenotype Ontology, patient support groups, and other NIH institutes and centers to compile comprehensive and understandable information.
NCATS Toolkit for Patient-Focused Therapy Development
View tools that can help patient groups advance medical research and patient-focused therapy development.
Related Research
Diagnostic Odyssey
This grant program funds the development of innovative approaches for reducing the time it takes to accurately diagnose rare diseases.
Rare Diseases Registry Program
This resource provides best practices for setting up and maintaining patient registries for research purposes.
Rare Diseases Clinical Research Network
We oversee this NIH-wide grant program that supports medical research on over 200 rare diseases through clinical studies, including collaborations, study enrollment and data sharing.