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Arrhythmogenic right ventricular dysplasia 4

MONDO:0011189

An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.

Also known as: ARVC4, ARVD4, arrhythmogenic right ventricular cardiomyopathy 4, arrhythmogenic right ventricular dysplasia type 4, fanilial arrhythmogenic right ventricular dysplasia 4, arrhythmogenic right ventricular dysplasia, familial, 4

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

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Broader categories

Cardiovascular disorder (1052) Disease (681) Heart disorder (301) Musculoskeletal system disorder (207) Hereditary disease (177) Cardiomyopathy (144) Muscle tissue disorder (56) Arrhythmogenic right ventricular cardiomyopathy (28) Intrinsic cardiomyopathy (16) Human disease (14)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 2
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  • Heart device data may unlock secrets of rare heart muscle disease

    Knowledge-focused Not yet recruiting

    This study looks back at the medical records of 300 people with arrhythmogenic cardiomyopathy who have an implantable cardioverter-defibrillator (ICD) and have had dangerous heart rhythms. Researchers want to count how often ICD-related problems occur, such as lead failure or ina…

    Sponsor: Policlinico Casilino ASL RMB • Aim: Knowledge-focused

    Last updated Jul 09, 2026 00:00 UTC

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