KMT2C Foundation

The KMT2C Foundation is a patient advocacy group championing clinical research for KMT2C chromosomal abnormalities. The Foundation firmly believes that no two families are going through the same medical journey and understands that the road to a diagnosis is often an emotional one. If you are a research-driven patient, family, or caregiver looking for community of peers, feel free to contact us. We are actively involved in an ongoing natural history study, medical surveys, and a bio-repository to work towards research and quality-of-life treatment options for our loved ones.