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

Registration for EAC 7 is now open!

It is a great pleasure to announce that the 7th European Aniridia Conference, that will be held in Stockholm, Sweden, on 31st May-2nd June 2023, has opened its registration platform. . The preliminary scientific programme is already defined and the list of speakers...

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EALA is looking for you! If you are 18 to 30, find out why

We are thrilled to introduce the European Aniridia Leadership Academy (EALA), a groundbreaking initiative brought to you by Aniridia Europe in collaboration with Aniridia Sweden. Our aim is to empower and equip young individuals with aniridia, aged 18 to 30, with the...

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