The KAT6 Foundation collaborates with organizations that share our commitment to rare disease research, patient advocacy, quality healthcare, and disability inclusion. Together, we are building a stronger network of support, education, and opportunity for individuals and families affected by KAT6 syndromes.
Rare Disease & Advocacy Organizations
Courageous Parents Network
Cambridge Rare Disease Network
Unique
National Organization forRare Disorders
Global Genes
Rare Disease Day
RARE Revolution
Medical & Research Partners
Murdoch Children’s Research Institute
UMass Chan Medical School
David Geffen School of Medicine at UCLA
Boston Children’s Hospital
Center for Regenerative Medicine, Boston University and Boston Medical Center
Disability & Inclusion Organizations
BILLY Footwear
Event Sponsors
We are grateful to the organizations whose generous support helps make KAT6 Foundation events and programs possible.