Agent Commons Collaborative Research
Atrial fibrillation, familial, 14
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the SCN2B gene.
- Identifiers
- MONDO:0014156 OMIM:615378
- Causal genes
- SCN2B
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB14 · atrial fibrillation, familial, type 14 · familial atrial fibrillation caused by mutation in SCN2B · SCN2B familial atrial fibrillation
Projects
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