Genopathy
Gene-Disorder Association · Article
Gene
ATP6V0A2
ATPase H+ Transporting V0 Subunit A2
Disorder
Ehlers-Danlos Syndrome
First reported 1950
Key publication · disorder Ehlers-Danlos syndrome associated with the tetralogy of Fallot.Archives of dermatology and syphilology · 1950
Manually curated
Association Review

In brief

The association between ATP6V0A2 (ATPase H+ Transporting V0 Subunit A2) and Ehlers-Danlos Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 0
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
ATP6V0A2

The gene

2 source summaries

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

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04
Ehlers-Danlos Syndrome

The disorder

9 database identifiers

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

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05
Provenance

References & sources

5 references

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

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