Genopathy
Gene-Disorder Association · Article
Gene
SCNN1G
Sodium Channel Epithelial 1 Subunit Gamma
Disorder
Pseudohypoaldosteronism
First reported 1995
Supporting publications 13
Key publication · gene–disorder Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis.The Journal of clinical endocrinology and metabolism · 1995
Key publication · disorder Pseudohypoaldosteronism.American journal of diseases of children (1960) · 1973
Manually curated
Association Review

In brief

The association between SCNN1G (Sodium Channel Epithelial 1 Subunit Gamma) and Pseudohypoaldosteronism is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 13
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
SCNN1G

The gene

1 source summary

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

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04
Pseudohypoaldosteronism

The disorder

7 database identifiers

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

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05
Literature

Reading

13 publications

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

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06
Provenance

References & sources

10 references

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

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