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Adams-Oliver syndrome 5

MONDO:0014459

Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the NOTCH1 gene.

Also known as: AOS5, Adams-Oliver syndrome 5, Adams-Oliver syndrome caused by mutation in NOTCH1, Adams-Oliver syndrome caused by mutation in Notch1, Adams-Oliver syndrome type 5

76 clinical trials for this condition and its sub-types, 0 tagged with Adams-Oliver syndrome 5 itself.

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↑ Non-syndromic limb reduction defect (35) ↑ NOTCH1-related AOS spectrum disorder (16) ↑ Adams-Oliver syndrome (0)
Including sub-types (76) Tagged with Adams-Oliver syndrome 5 (0)
Trials to join now! 34 Not yet recruiting 12 Not yet finished but already full! 11 Completed 18 Terminated 1
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  • App-Based exercise program aims to strengthen hearts in congenital disease

    Disease control Stopped early

    This study tests a remote, app-enabled exercise program designed for people aged 10 to 50 with congenital heart disease. Participants use a smartphone app with exercise modules and wearable devices to track heart rate and progress. The goal is to see if this approach can safely i…

    Sponsor: Duke University • Aim: Disease control

    Last updated Aug 07, 2026 00:00 UTC

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