Genopathy
Gene-Disorder Association · Article
Gene
FOXE3
Forkhead Box E3
Disorder
Anterior Segment Dysgenesis
First reported 2009
Supporting publications 14
Key publication · gene–disorder Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.Human mutation · 2009
Key publication · disorder The story of ASGD. What it's all about.The Journal of the American Society for Geriatric Dentistry · 1975
Manually curated
Association Review

In brief

The association between FOXE3 (Forkhead Box E3) and Anterior Segment Dysgenesis is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 334
Symptoms 0
Compounds 0
Trials 0
Publications 14
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

2 sources

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

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03
FOXE3

The gene

1 source summary

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

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04
Anterior Segment Dysgenesis

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
ClinVar and variant evidence

Genetic basis

334 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

14 publications

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

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07
Provenance

References & sources

12 references

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

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