Orphanet Rare Disease Ontology

Last uploaded: December 13, 2023
Preferred Name

Familial atrial fibrillation

Synonyms
Definitions

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.

ID

http://www.orpha.net/ORDO/Orphanet_334

definition

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.

definition_citation

Orphanet

expertlink

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

hasDbXref

MedDRA:10088317

OMIM:608583

OMIM:612201

UMLS:C3468561

OMIM:613055

ICD-11:BC65.Y

OMIM:607554

OMIM:617280

OMIM:614050

OMIM:613980

OMIM:608988

OMIM:615377

OMIM:615378

OMIM:613120

OMIM:611493

OMIM:611494

OMIM:614022

OMIM:614049

OMIM:612240

OMIM:611819

ICD-10:I48.9

OMIM:615770

label

Familial atrial fibrillation

notation

ORPHA:334

part_of

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

prefixIRI

ORDO:Orphanet_334

prefLabel

Familial atrial fibrillation

treeView

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

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

Delete Subject Author Type Created
No notes to display