At the CGD Society, the research we fund is cutting-edge. It is an exciting area for CGD-affected individuals but for millions of other people, too. Research into single-gene deficiencies like CGD can yield results that can also shed light on how other genetic disorders work.

Whether you are a researcher or a layperson looking for more information on groundbreaking work into CGD, or an academic looking to apply for a grant, we are here to help.

Share this page

IMPORTANT NOTE: The information contained on this website is intended only as a guideline, not as a substitute for medical advice. Always consult your doctor if you or your child has any CGD symptoms or concerns.