fetal loss, late Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group cardiovascular (Genetic Association Database)
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Genes

13 genes associated with the disease fetal loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
APOB apolipoprotein B
APOE apolipoprotein E
F13A1 coagulation factor XIII, A1 polypeptide
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FGB fibrinogen beta chain
HFE hemochromatosis
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
PROCR protein C receptor, endothelial
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
THBD thrombomodulin