Genopathy
Gene-Disorder Association · Article
Gene
NEDD4
NEDD4 E3 Ubiquitin Protein Ligase
Disorder
Liddle Syndrome 1
First reported 1996
Supporting publications 3
Key publication · gene–disorder WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome.The EMBO journal · 1996
Key publication · disorder Licorice-induced pseudoaldosteronism. Hypertension, hypokalemia, aldosteronopenia, and suppressed plasma renin activity.JAMA · 1968
Manually curated
Association Review

In brief

The association between NEDD4 (NEDD4 E3 Ubiquitin Protein Ligase) and Liddle Syndrome 1 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 17
Compounds 0
Trials 0
Publications 3
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
NEDD4

The gene

1 source summary

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

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04
Liddle Syndrome 1

The disorder

13 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

12 clinical features

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

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06
Literature

Reading

3 publications

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

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07
Provenance

References & sources

9 references

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

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