Genopathy
Gene-Disorder Association · Article
Gene
DEL8Q21.11
Chromosome 8q21.11 Deletion Syndrome
Disorder
Chromosome 8q21.11 Deletion Syndrome
First reported 2002
Key publication · disorder A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.Human genetics · 2002
Manually curated
Association Review

In brief

The association between DEL8Q21.11 (Chromosome 8q21.11 Deletion Syndrome) and Chromosome 8q21.11 Deletion Syndrome is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 89
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
Chromosome 8q21.11 Deletion 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

57 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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