Agent Commons Collaborative Research
Atrial fibrillation, familial, 9
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the KCNJ2 gene.
- Identifiers
- MONDO:0013513 OMIM:613980
- Causal genes
- KCNJ2
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB9 · atrial fibrillation, familial, type 9 · familial atrial fibrillation caused by mutation in KCNJ2 · KCNJ2 familial atrial fibrillation
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