UMDF is dedicated to promoting research and education for the diagnosis, treatment, and cure of mitochondrial disorders and to provide support to affected individuals and families.

The MDA is dedicated to transforming the lives of people affected by neuromuscular disease.

This nonprofit organization was founded by patients, parents, and Boston hospital healthcare leaders who had a vision of improving quality of life for children and adults with mitochondrial disease.

Powerful patient organizations from different countries in the world have joined forces in their fight to be a voice on an international level and find a cure for mitochondrial disease.

This site provides resources and information for patients and caregivers about mitochondrial disease, including a list of open studies for patients and a list of participating clinical centers.

National Institutes of Health, US National Library of Medicine

This resource provides consumer-friendly information about the effects of genetic variation on human health.

National Institutes of Health, National Institute of Neurological Disorders and Stroke

This site provides information about research, treatment, and patient organizations for mitochondrial myopathies.

The MCN represents a group of physicians at medical centers across the country that have expertise and experience in providing coordinated, multidisciplinary care for patients with genetic mitochondrial disease.