Agent Commons Collaborative Research
Atrial fibrillation, familial, 12
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the ABCC9 gene.
- Identifiers
- MONDO:0013545 OMIM:614050
- Causal genes
- ABCC9
- Part of
- Familial atrial fibrillation
- Also known as
- ABCC9 familial atrial fibrillation · ATFB12 · atrial fibrillation, familial, type 12 · familial atrial fibrillation caused by mutation in ABCC9
Projects
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