Genopathy
Gene-Disorder Association · Article
Gene
POU3F4
POU Class 3 Homeobox 4
Disorder
Autosomal Dominant Nonsyndromic Hearing Loss 3a
First reported 1997
Key publication · disorder Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.Nature · 1997
Manually curated
Association Review

In brief

The association between POU3F4 (POU Class 3 Homeobox 4) and Autosomal Dominant Nonsyndromic Hearing Loss 3a is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
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
POU3F4

The gene

1 source summary

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

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04
Autosomal Dominant Nonsyndromic Hearing Loss 3a

The disorder

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

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05
Provenance

References & sources

2 references

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

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