Genopathy
Gene-Disorder Association · Article
Gene
LMNA
Lamin A/C
Disorder
Atrial Fibrillation
First reported 2009
Supporting publications 4
Key publication · gene–disorder A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death.Heart rhythm · 2009
Key publication · disorder Atrial fibrillation as a self-sustaining arrhythmia independent of focal discharge.American heart journal · 1959
Manually curated
Association Review

In brief

The association between LMNA (Lamin A/C) and Atrial Fibrillation is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 4
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
LMNA

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Atrial Fibrillation

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Literature

Reading

4 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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06
Provenance

References & sources

7 references

Every source and publication cited across this dossier, as one numbered reference list.

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