Mighty Mito

COX20 Community

Have COX20? We'd love to hear from you.

Do you or someone in your family have a COX20-related mitochondrial disorder? We'd love to connect.

Whether you're newly diagnosed, have been navigating COX20 deficiency for years, or are simply looking for others who understand, you're welcome here.

With your permission, Mighty Mito may contact you if another COX20 family is interested in connecting. We will never share your information without your consent.