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Dilated cardiomyopathy 1HH

MONDO:0013479

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the BAG3 gene.

Also known as: BAG3 familial isolated dilated cardiomyopathy, CMD1HH, cardiomyopathy, dilated, type 1Hh, dilated cardiomyopathy type 1HH, familial isolated dilated cardiomyopathy caused by mutation in BAG3, cardiomyopathy, dilated, 1HH

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

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Musculoskeletal system disorder (207) Hereditary disease (176) Cardiomyopathy (144) Dilated cardiomyopathy (72) Muscle tissue disorder (56) Intrinsic cardiomyopathy (16) Human disease (14)
Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 3
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  • Tiny study could unlock secrets of genetic heart failure

    Knowledge-focused Not yet recruiting

    This study follows 10 Chinese adults who have a specific gene mutation (BAG3) linked to dilated cardiomyopathy, a condition where the heart becomes enlarged and weak. Researchers will track changes in heart function, symptoms, and biomarkers over time to better understand how the…

    Sponsor: AstraZeneca • Aim: Knowledge-focused

    Last updated Jun 27, 2026 14:00 UTC

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