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

The 7th European Aniridia Conference announced!

Aniridia Sweden together with Linköping University and Aniridia Europe are proud to announce the 7th European Aniridia Conference (EAC) that will take place in Stockholm, Sweden on May 31st – June 2nd, 2024. The scientific programme for the 2024 EAC is...

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Greetings from the new Board

Dear friends, Aniridia Europe's General Assembly, held online on 13th July 2022, has elected a new Board of Directors and the other organs of the federation. You can meet the new Board on the trustees' page, and read the minutes of the assembly on our website. The new...

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