Rare Genomics Institute connects patients to research institutions and assists with logistics and fundraising.
Rare Genomics Institute (RGI) is a non-profit organization dedicated to helping rare disease patients find hope through cutting-edge research and personalized medicine. RGI empowers patients and families by providing access to genomic sequencing, research funding, and a supportive community to navigate the challenges of rare diseases.
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Programs designed to empower patients and families affected by rare diseases through education, resources, and support.
Facilitates access to genomic sequencing technologies for patients to help identify the genetic causes of their rare diseases.
Provides funding for research projects aimed at understanding and treating rare diseases.
Offers a supportive community for patients and families to share experiences, advice, and hope.
Comprehensive resources on rare diseases, genomics, and the latest in medical research.
Works closely with researchers and scientists to advance the understanding and treatment of rare diseases.
Advocates for policies and initiatives that support rare disease research and patient care.
To empower rare disease patients with the tools to find customized treatment options through genomic research.
A world where every rare disease patient has access to personalized medicine and the hope for a cure.
RGI has helped hundreds of patients and families worldwide, funding numerous research projects and providing critical support services.
Individuals can support RGI through donations, volunteering, or participating in fundraising events.
For more information, visit the website at raregenomics.org or contact via email at info@raregenomics.org.
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