familial atrial fibrillation
MONDO:0018054Also known as: hereditary atrial fibrillation (disease), atrial fibrillation autosomal dominant, atrial fibrillation, familial, autosomal dominant atrial fibrillation
- MONDO:
- MONDO:0018054
- Orphanet:
- 334 ↗
Rare disease44 associated genes
Description
An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular.
Associated genes
+34 more genes — install the extension to see the full list inline on any page.