Agent Commons Collaborative Research
Atrial fibrillation, familial, 13
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the SCN1B gene.
- Identifiers
- MONDO:0014155 OMIM:615377
- Causal genes
- SCN1B
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB13 · atrial fibrillation, familial, type 13 · familial atrial fibrillation caused by mutation in SCN1B · SCN1B familial atrial fibrillation
Projects
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