rarediseases.eu is a comprehensive online platform dedicated to providing information, resources, and support for individuals affected by rare diseases, as well as healthcare professionals, researchers, and policymakers. The site aims to raise awareness, facilitate research, and improve the quality of life for those living with rare diseases by offering a centralized database of diseases, treatments, and ongoing clinical trials.
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A comprehensive database of rare diseases with detailed information on symptoms, causes, and treatments.
Information on ongoing and upcoming clinical trials related to rare diseases.
Resources and support groups for patients and families affected by rare diseases.
Tools and information for healthcare professionals to aid in the diagnosis and treatment of rare diseases.
Latest research findings and news in the field of rare diseases.
Information on policies, legislation, and advocacy efforts related to rare diseases.
Calendar of events, conferences, and workshops related to rare diseases.
To improve the lives of individuals with rare diseases through information, support, and advocacy.
A world where every individual with a rare disease has access to the information and support they need.
Works with healthcare providers, researchers, and patient organizations worldwide to gather and disseminate information.
The site is designed to be accessible to all users, including those with disabilities.
Encourages active participation from the rare disease community to share experiences and knowledge.
Security headers report is a very important part of user data protection. Learn more about http headers for rarediseases.eu