Atrial fibrillation, familial, 13

MONDO:0014155

Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN1B gene.

Also known as: SCN1B familial atrial fibrillation, atrial fibrillation, familial, 13, atrial fibrillation, familial, type 13, familial atrial fibrillation caused by mutation in SCN1B, ATFB13

30 clinical trials for this condition and its sub-types, 0 tagged with Atrial fibrillation, familial, 13 itself.

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↑ Familial atrial fibrillation (1)

Including sub-types (30) Tagged with Atrial fibrillation, familial, 13 (0)

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