/atrial fibrillation, familial, 13

atrial fibrillation, familial, 13

Rare Disease

MONDO:0014155

Also Known As

SCN1B familial atrial fibrillationatrial fibrillation, familial, 13atrial fibrillation, familial, type 13familial atrial fibrillation caused by mutation in SCN1BATFB13

Definition

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

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Associated Genes

SCN1B ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615377 ↗

GARD

GARD:15954 ↗

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