Genopathy
Gene-Disorder Association · Article
Gene
GJB6
Gap Junction Protein Beta 6
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 GJB6 (Gap Junction Protein Beta 6) 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
GJB6

The gene

2 source summaries

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

3 references

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

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