Gene-Disorder Association · Article
First reported
1995
Supporting publications
102
Manually curatedApproved treatment annotated
Association Review
In brief
The association between PON1 (Paraoxonase 1) and Coronary Artery Anomaly is reported, with clinical genetic testing available.
Sources
1
Clinical variants
0
Symptoms
7
Compounds
1
Trials
83of 898 via PON1 compounds
Publications
102
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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1 source summary
A gene summary alongside the source descriptions it was distilled from.
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04
Coronary Artery Anomaly
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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05
Interventions
Therapeutics
1 compound or drug
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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06
Human studies
Clinical trials
898 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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102 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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08
Provenance
References & sources
13 references
Every source and publication cited across this dossier, as one numbered reference list.
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