Atrial fibrillation, familial, 13

Definition

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

Also known as atrial fibrillation, familial, 13, atrial fibrillation, familial, type 13, familial atrial fibrillation caused by mutation in SCN1B, SCN1B familial atrial fibrillation — per MONDO

Also identified as

• OMIM 615377 per MONDO
• UMLS C3809311 per MONDO