Orphanet: Familial atrial fibrillation

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Familial atrial fibrillation

Disease 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.

ORPHA:334

Classification level: Disorder

Synonym(s): -
Prevalence: -
Inheritance: Autosomal dominant
Age of onset: Adult, Elderly
ICD-10: I48.9
ICD-11: BC65.Y
OMIM: 607554 608583 608988 611493 611494 611819 612201 612240 613055 613120 613980 614022 614049 614050 615377 615378 615770 617280
UMLS: C3468561
MeSH: -
GARD: 9740
MedDRA: 10088317

Detailed information

Guidelines

Clinical practice guidelines
English (2013) - Europace
Deutsch (2013) - AWMF
Français (2014) - ALD

Clinical Outcome Assessment (COA)

Patient-Centered Outcome Measures (PCOMs)
English (2023) - PROQOLID^TM

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Familial atrial fibrillation

ORPHA:334

A summary on this disease is available in Deutsch (2017) Español (2017) Français (2017) Italiano (2017) Nederlands (2017)

Guidelines

Clinical Outcome Assessment (COA)

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening