Albinism International Databank (AID)

Serving the Global Albinism Community


This is a free platform to share your journey and further research.  Join now!

For more information about how to register, click here.

For Researchers

Drive Research

This is a unique rare disease patient registry. Are you interested in using our data to further your rare disease research?

For Participants

Get Involved

Information collected during this study may be used to help provide opportunities for patients and researchers to collaborate in the rare disease community.