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epilepsy

Disease Summary
Associated Targets (483)
Tbio

262

Tclin

126

Tchem

87

Tdark

8


Disease Ontology Description A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.
DataSource References
DisGeNET: C0014544
JensenLab Knowledge UniProtKB-KW: DOID:1826
CTD: DOID:1826
JensenLab Text Mining: DOID:1826
DrugCentral Indication: DOID:1826
Monarch: DOID:1826
GWAS Targets (7)
Target
TDL
Study Count
SNP Count
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tclin
2
2
0
4.2
84.8
Tbio
1
1
0
1.6
59.5
Tchem
1
1
0
1.1
44
Tdark
1
1
0
14
31.8
Tclin
1
1
0
1.4
31.4
Target
TDL
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tclin
0
4.2
84.8
Tbio
0
1.6
59.5
Tchem
0
1.1
44
Tdark
0
14
31.8
Tclin
0
1.4
31.4
Target Novelty (Tin-x)