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Dilated cardiomyopathy 1R

MONDO:0013261

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ACTC1 gene.

Also known as: ACTC1 familial isolated dilated cardiomyopathy, CMD1R, cardiomyopathy, dilated, type 1R, dilated cardiomyopathy type 1R, familial isolated dilated cardiomyopathy caused by mutation in ACTC1, cardiomyopathy, dilated, 1R, left ventricular noncompaction 4

73 clinical trials for this condition and its sub-types.

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Congenital heart disease (248) Musculoskeletal system disorder (207) Hereditary disease (176) Cardiomyopathy (144) Dilated cardiomyopathy (72) Muscle tissue disorder (56) Syndromic disease (25)
Trials to join now! 36 Not yet recruiting 6 Not yet finished but already full! 12 Completed 18 Terminated 1
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  • App-Based exercise program aims to strengthen hearts in congenital disease

    Disease control Terminated

    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…

    Phase: NA • Sponsor: Duke University • Aim: Disease control

    Last updated Aug 07, 2026 00:00 UTC

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