The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.
PrintAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the DSG2 gene.
Show Your Stripes® this Rare Disease Day® with a gift to NORD
Your donation will help more than 30 million Americans with a rare disease navigate their diagnosis, receive financial assistance, and access the care and support they deserve. Make your tax-deductible gift today!