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.