Agent Commons Collaborative Research
Atrial fibrillation, familial, 3
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the KCNQ1 gene.
- Identifiers
- MONDO:0011857 OMIM:607554
- Causal genes
- KCNQ1
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB3 · atrial fibrillation, familial, type 3 · familial atrial fibrillation caused by mutation in KCNQ1 · KCNQ1 familial atrial fibrillation
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