Genopathy
Gene-Disorder Association · Article
Gene
SCNN1A
Sodium Channel Epithelial 1 Subunit Alpha
Disorder
Liddle Syndrome 3
First reported 1994
Key publication · disorder Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel.Cell · 1994
Manually curated
Association Review

In brief

The association between SCNN1A (Sodium Channel Epithelial 1 Subunit Alpha) and Liddle Syndrome 3 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.

Sources 4
Clinical variants 140
Symptoms 7
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

4 sources

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

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03
SCNN1A

The gene

1 source summary

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

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04
Liddle Syndrome 3

The disorder

6 database identifiers

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

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05
Phenotype

Clinical features

5 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

140 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Provenance

References & sources

6 references

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

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