A group image from the second Aniridia Europe's conference in Venice in 2014

Aniridia Europe gathers people all over the continent

 

We want to support people with aniridia in all countries and help them to share information and build useful networks in their own countries and abroad.

 

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What is 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 September 2021, the federation includes 13 national associations, as well as support groups and contact persons in 20 other European countries.
Get in touch with someone in your country.

An image of two girls with aniridia smiling on Summer Camp
A image of a group of young people with aniridia from Summer Camp in 2015
A portrait image of a girl with aniridia
An image of a young girl with aniridia who smiling in front of the camera

News & Events

Aniridia and WAGR patient brochures published in Russia

When you are dealing with a rare disease such as aniridia, there is a lot of information that you come across in a short time, and it is really difficult to understand what are the most important things that you need to know and to do, and in which priority order....

Learn more