Familial atrial fibrillation is a rare, genetically heterogenous cardiac disease characterized by erratic activation of the atria with an irregular ventricular response, in various members of a single family. It may be asymptomatic or associated with palpitations, dyspnea and light-headedness. Concomitant rhythm disorders and cardiomyopathies are frequently reported.

This is just here as a test because I lose it

Term information

database cross reference
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=334

hasDbXref

OMIM:611819

OMIM:617280

OMIM:608988

ICD-10:I48.9

OMIM:614050

OMIM:615770

OMIM:614022

OMIM:612240

OMIM:613120

OMIM:611494

OMIM:615378

OMIM:613055

OMIM:611493

OMIM:615377

OMIM:613980

OMIM:612201

OMIM:614049

OMIM:607554

OMIM:608583

has inheritance

http://www.orpha.net/ORDO/Orphanet_409929

notation

ORPHA:334

part of

http://www.orpha.net/ORDO/Orphanet_101934