The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.
The mission of the FOXG1 Research Foundation is to accelerate research to find a cure for FOXG1 syndrome. We will fund the world's leading scientists that are integral along our Path to a Cure for all children with FOXG1 syndrome. We will continue to apply our research to solve all related brain disorders. FOXG1 is the super hero "master regulator" gene that could save millions of children with various brain disorders. We will not stop until every stone is unturned. We are dedicated to:
Please Note
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.
