Gene-Disorder Association · Article
Gene
NR3C1 Nuclear Receptor Subfamily 3 Group C Member 1
×
First reported
1990
Supporting publications
4
Manually curated Approved treatment annotated
Association Review
In brief The association between NR3C1 (Nuclear Receptor Subfamily 3 Group C Member 1) and Primary Hyperaldosteronism is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.
Sources
1
Clinical variants
0
Symptoms
68
Compounds
4
Trials
27 of 3,311 via NR3C1 compounds
Publications
4
Contents
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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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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A gene summary alongside the source descriptions it was distilled from.
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Primary Hyperaldosteronism
The disorder 21 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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Phenotype
Clinical features 64 clinical features
The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.
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Mechanism overlap
Shared mechanisms Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.
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Interventions
Therapeutics 4 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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Human studies
Clinical trials 3,311 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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Provenance
References & sources 12 references
Every source and publication cited across this dossier, as one numbered reference list.
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