The most noticeable symptom of aniridia is the partial or complete lack of an iris in both eyes.
Representatives of European Aniridia Associations gather at the 3rd European Conference on Aniridia in 2016
Youths with aniridia rafting at One Vision! Summer Camp 2015
One of our mission objectives is to spread information and inspire research on aniridia.
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.
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News & events
- Report on the webinar “News from the frontier”, 27th February 2021
- 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