Whether you're new to the duchenne registry or looking for an upgrade, our curated collection of 210+ iOS apps has something for everyone. Each app is reviewed and rated by real users, helping you make an informed decision.
Compare top The Duchenne Registry Apps (April 2026)
This app collects data from individuals diagnosed with Duchenne or Becker muscular dystrophy, and their carriers. It aims to make this information searchable for clinicians and researchers to advance understanding and speed up trials. Users can access information on relevant clinical trials and research studies.
This app provides critical emergency care information, research news, and advocacy alerts for Duchenne muscular dystrophy. It connects users to the Duchenne community and offers educational tools for parents and caregivers.
This app is a large online health community offering resources and peer support for various health conditions, including mental health, chronic illness, and neurodiversity. Users can read personal stories, find curated resources, connect with others in support groups, and share their own experiences.
What are the best the duchenne registry apps for iPhone?
The Duchenne Registry tops our the duchenne registry apps ranking as of April 2026, with a 5.0-star average from 5 App Store ratings, and it's free to download.
Are there free the duchenne registry apps for iPhone?
Yes — 20 of the top the duchenne registry apps we rank are free to download, including The Duchenne Registry and Parent Project MD.
Does The Duchenne Registry have ads or in-app purchases?
The Duchenne Registry has no ads and has no in-app purchases, according to its App Store listing as of April 2026.
How many the duchenne registry apps are on the App Store?
We track 210+ the duchenne registry apps on the iOS App Store as of April 2026, ranked by rating, recency, and analysis of real user reviews.
What is The Duchenne Registry?
The Duchenne Registry is a platform designed for individuals diagnosed with Duchenne or Becker muscular dystrophy, and their carriers. It collects and securely shares de-identified data with researchers and clinicians to advance understanding and treatment of these conditions.
Who can register for The Duchenne Registry?
Individuals diagnosed with Duchenne or Becker muscular dystrophy, carriers of these conditions, and parents or guardians registering on behalf of children and teens can participate. Caregivers of adults with these conditions can also assist with registration.