Eclampsia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A pre-eclampsia characterized by the presence of seizures. (Human Disease Ontology, DOID_13593)
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16 genes associated with the Eclampsia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HLA-G major histocompatibility complex, class I, G
IL10 interleukin 10
IL6 interleukin 6
LTA lymphotoxin alpha
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
SCNN1B sodium channel, non voltage gated 1 beta subunit
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor