About the Disease

Duchenne muscular dystrophy (DMD), also known as Duchenne syndrome, is a genetic disease characterized by progressive muscle weakness and degeneration primarily in the skeletal and cardiac muscles. It is a rare disease that affects the musculoskeletal system.

Source: National Institutes of Health

Related Organizations

Diagnosis Codes

ICD-10: G71.01

Clinical Trials

If you’ve ever wondered how to sign up for a clinical trial but aren’t sure where to start, visit PAN Foundation’s education hub to learn about safety, compensation, and more. Read real stories from patients who participated in clinical trials, find a clinical trial that matches your interest, and call us to talk to a ComPANion Access Navigator for free, personalized help.