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Rare diseases website for patients.

EURORDIS is a non-governmental patient-driven alliance of patient organizations representing 837 rare disease patient organizations in 70 countries. We are the voice of 30 million people affected by rare diseases throughout Europe.

Type of information: Drugs;Compasionate Use;Treatment Options;Personal Opinions;Blogs;Support Groups

Type of question: Treatments;Clinical Trials;Experts
Disease: Rare Diseases
Access type: Open access
Relevancy: High

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