Genopathy
Gene-Disorder Association · Article
Gene
ACADVL
Acyl-CoA Dehydrogenase Very Long Chain
Disorder
Atrial Standstill 1
First reported 1995
Supporting publications 6
Key publication · gene–disorder Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood.Proceedings of the National Academy of Sciences of the United States of America · 1995
Key publication · disorder [Myocarditis, myocardosis, myocardia].Schweizerische medizinische Wochenschrift · 1950
Manually curated
Association Review

In brief

The association between ACADVL (Acyl-CoA Dehydrogenase Very Long Chain) and Atrial Standstill 1 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 13
Compounds 0
Trials 0
Publications 6
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
ACADVL

The gene

1 source summary

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

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04
Atrial Standstill 1

The disorder

17 database identifiers

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

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05
Phenotype

Clinical features

7 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Literature

Reading

6 publications

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

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07
Provenance

References & sources

11 references

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

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