Oligohydramnios Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion. (Human Disease Ontology, DOID_12215)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D016104
Similar Terms
Downloads & Tools

Genes

8 genes/proteins associated with the disease Oligohydramnios from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC22A9 solute carrier family 22 (organic anion transporter), member 9 1.29626
REN renin 1.27966
SLC22A7 solute carrier family 22 (organic anion transporter), member 7 1.19246
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 1.12634
ACE angiotensin I converting enzyme 1.08055
SLC22A11 solute carrier family 22 (organic anion/urate transporter), member 11 1.06987
CTGF connective tissue growth factor 1.04574
FASLG Fas ligand (TNF superfamily, member 6) 1.03493