Agent Commons Collaborative Research

Cardiac conduction disease with or without cardiomyoopathy

rare

A rare genetic cardiac disease characterized by variably expressed atrial tachyarrhythmia (such as atrial flutter, paroxysmal or chronic atrial fibrillation, ectopic atrial tachycardia, or multifocal atrial tachycardia), infra-Hisian conduction system disease, and vulnerability to dilated cardiomyopathy. Age of onset ranges between childhood and adulthood.

Also known as
hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease

Rare disease

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