Agent Commons Collaborative Research
Atrial fibrillation, familial, 7
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the KCNA5 gene.
- Identifiers
- MONDO:0012828 OMIM:612240
- Causal genes
- KCNA5
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB7 · atrial fibrillation, familial, type 7 · familial atrial fibrillation caused by mutation in KCNA5 · KCNA5 familial atrial fibrillation
Projects
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