placental abruption Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A placenta disease that is characterized by separation of the placental lining from the uterus of the mother. (Human Disease Ontology, DOID_9667)
Similar Terms
Downloads & Tools

Genes

3 genes associated with the disease placental abruption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
NOS3 nitric oxide synthase 3 (endothelial cell)
THBD thrombomodulin