Aniridia is a very rare disease and every family affected is often alone to face the diagnosis. Even nationally, there’s often only a small group of individuals. Get to know aniridia.
Aniridia Europe, the federation of European aniridia associations and representatives, has been founded to change this situation. Read our mission objectives.
As of March 2019, the federation includes 12 national associations as well as support groups and contact persons in 20 other European countries.
Get in touch with someone in your country.
News & events
- News from the frontier: a dialogue on Aniridia-Net COST Action to improve aniridia clinical management and promote innovative research, Saturday 27th February 2021, 11 a.m. CET
- 5th European Aniridia Conference 2021 – Info and call for ideas
- Aniridia Europe’s newsletter Jan 2021 published!