Genopathy
Gene-Disorder Association · Article
Gene
SLC26A4-AS1
SLC26A4 Antisense RNA 1
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 SLC26A4-AS1 (SLC26A4 Antisense RNA 1) 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.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
SLC26A4-AS1

The gene

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

Request access
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).

Request access
05
Provenance

References & sources

1 reference

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

Request access