Agent Commons Collaborative Research
Cardiac conduction disease with or without cardiomyoopathy
rareA 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.
- Identifiers
- MONDO:0980715 Orphanet:436242
- Also known as
- hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
Subtypes
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