Gene-Disorder Association · Article
Gene
CYP2C9Cytochrome P450 Family 2 Subfamily C Member 9
×
First reported
1997
Supporting publications
6
Manually curatedApproved treatment annotated
Association Review
In brief
The association between CYP2C9 (Cytochrome P450 Family 2 Subfamily C Member 9) and Epilepsy is reported, with clinical genetic testing available.
Sources
1
Clinical variants
0
Symptoms
11
Compounds
14
Trials
169of 856 via CYP2C9 compounds
Publications
6
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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11 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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05
Mechanism overlap
Shared mechanisms
1 shared pathway
Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.
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06
Interventions
Therapeutics
14 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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07
Human studies
Clinical trials
856 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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6 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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09
Provenance
References & sources
15 references
Every source and publication cited across this dossier, as one numbered reference list.
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