RG gives rare disease patients access to modern genomics sequencing technology, connections to scientists and researchers and philanthropic opportunities. Shortening the diagnostic odyssey is our core mission. To apply as a new patient, click here: raregenomics.org/how-we-help-pa…
Rare Genomics
@RareGenomics
RGI is a non-profit organization that provides research to families in need of diagnosis & treatment for rare genetic diseases.
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RGs' Patient Research Services (RGPRS) connects rare disease patients to genomic research. When Ally’s family sought answers, RGPRS analyzed her genome and identified a histone-4 variant (H4C5) explaining her symptoms. Enroll as a new patient here: loom.ly/qt9fAv4
February 28th is Rare Disease Day! This global movement raises awareness for rare diseases and highlights the urgent need for research, innovation, and advocacy.
Join us in the lead-up to #RareDiseaseDay by spreading awareness and supporting the rare disease community. 💡💜
Join us in the lead-up to #RareDiseaseDay by spreading awareness and supporting the rare disease community. 💡💜
Our president and CEO Jimmy Lin discusses groundbreaking technological advancements in artificial intelligence and machine learning to help beat cancer! Watch the symposium to learn more about the innovation at the leading edge of cancer science.
💜 We’re counting down to Rare Disease Day on February 28, 2025! Over 300 million people worldwide live with a rare disease—yet many still lack a diagnosis and treatment.
At @RareGenomics, we’re committed to empowering families with genomic insights and expert connections.
At @RareGenomics, we’re committed to empowering families with genomic insights and expert connections.
The number of people living with a rare disease is equivalent to the third largest country in the world. 🌎View quoted post on X
On #RareDiseaseDay, we aim to highlight their voices and raise awareness about their experiences.
Download our Infographics: rarediseaseday.org/downloads/