Genopathy
Gene-Disorder Association · Article
Gene
DUP7Q11.23
Chromosome 7q11.23 Duplication Syndrome
Disorder
Williams-Beuren Region Duplication Syndrome
First reported 1986
Key publication · disorder Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma.Cancer genetics and cytogenetics · 1986
Manually curated
Association Review

In brief

The association between DUP7Q11.23 (Chromosome 7q11.23 Duplication Syndrome) and Williams-Beuren Region Duplication Syndrome is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 163
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
Williams-Beuren Region Duplication 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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04
Phenotype

Clinical features

111 clinical features

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

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05
Provenance

References & sources

4 references

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

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