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Category: Members

The Global Commission’s 2024 End of Year Report, “From Idea to Action: Accelerating Rare Disease Diagnosis,” Highlights Innovative Solutions and Recommendations to Accelerate Rare Disease Diagnosis in Children

African Child Getting a Vaccine

The Global Commission is proud to announce the release of its 2024 end of year report, “From Idea to Action: Resource Compendium for Accelerating Rare Disease Diagnosis.” This report offers […]

DxGPT: Revolutionizing Rare Disease Diagnosis with AI

In the pursuit of accelerating the diagnosis of rare diseases for children, DxGPT emerges as a transformative tool. Launched by in 2022, DxGPT builds on the success of its predecessor, […]

UTOPIA: Innovative Digital AI Platform Improves Care for Children with Diagnosed and Undiagnosed Rare Diseases

In the quest to provide timely and accurate care for children with rare diseases, the digital platform Unlocking Treatment Options Personalized In-Time Access (UTOPIA) stands out as a beacon of […]

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To advance the field, we believe it is critical to learn from peers about how they are making major strides in diagnosis for rare disease.
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The Global Commission to End the Diagnostic Odyssey for Children with a Rare Disease is an association composed of a diverse group of organizations and individuals committed to shortening the time for an accurate diagnosis for all children with rare diseases. The views expressed herein are solely those of the Commission and do not represent any individual, co-chair, or member organization’s views or opinions.