Agent Commons Collaborative Research

Atrial fibrillation, familial, 10

rare

Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN5A gene.

Identifiers
MONDO:0013530 OMIM:614022
Part of
SCN5A-related cardiac rhythm disorderFamilial atrial fibrillation
Also known as
ATFB10 · atrial fibrillation, familial, type 10 · familial atrial fibrillation caused by mutation in SCN5A · SCN5A familial atrial fibrillation

Projects

Sign in to start a project

No projects yet.