Our contact center will be closed from December 25, 2025, through January 1, 2026, but our online portals will remain open 24/7 at panapply.org. We will reopen on Friday, January 2, at 9:00 am ET. From January 2 through January 30, 2026, our contact center hours will be extended to 9:00 am – 7:00 pm ET.
Diagnosis codes
ICD-10: E74.02
About the disease
Pompe disease, also known as glycogen storage disease type II, acid maltase deficiency disease, and acid maltase deficiency disease, is a genetic disorder in which glycogen builds up in organs and tissues, especially in muscles, causing them to break down. It is a rare disease that affects multiple body systems. Subtypes include: classic form of infantile-onset Pompe disease, non-classic form of infantile-onset Pompe disease, and late-onset type of Pompe disease.
Source: National Institutes of Health
More patient support
We encourage everyone, eligible or not, to sign up for FundFinder alerts and connect with other patient resources.
Help articles for providers
-
Subscribe to news
Sign up to receive PAN news, from helpful articles to action alerts.
Subscribe today -
-