Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype BEFREE In conclusion, DES is a potent HSD11B2 inhibitor, possibly contributing to the intrauterine growth restriction. 31247589 2019
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype BEFREE Placental 11β-hydroxysteroid dehydrogenase 2 (11β-HSD2), a glucocorticoid-catalyzing enzyme, prevents active glucocorticoids from maternal circulation into the fetus, thus protecting against IUGR. 31315888 2019
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 AlteredExpression phenotype BEFREE It appears that different causes of IUGR may attenuate HSD11B2 expression differentially in the placenta. 30225585 2019
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 AlteredExpression phenotype BEFREE It is known that inhibiting 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) expression in the placenta can cause fetal over-exposure to maternal glucocorticoids and induce intrauterine growth restriction (IUGR); these effects ultimately increase the risk of adult chronic diseases. 29802914 2018
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 AlteredExpression phenotype BEFREE Impaired placental 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) activity which inactivates maternal glucocorticoids is associated with poor fetal growth and a higher risk of chronic diseases in adulthood. 29486207 2018
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 PosttranslationalModification phenotype BEFREE In addition, significantly elevated odds of FGR birth were associated with increasing DNA methylation of HSD11B2 and WNT2, and decreasing DNA methylation of IGF2. 26678531 2016
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 PosttranslationalModification phenotype BEFREE These results together show a link between the site-specific methylation of placental HSD11B2 promoter and the development of IUGR. 24129435 2014
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 AlteredExpression phenotype BEFREE In conclusion, placental 11beta-HSD2 gene expression might predict postnatal growth in IUGR. 19218882 2009
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 AlteredExpression phenotype BEFREE 11beta-HSD1 protein levels were reduced in amnion and 11beta-HSD1 and 11beta-HSD2 oxidase activity in decidua and cotyledon were reduced from pregnancies with IUGR. 19776596 2009
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype BEFREE Taken together, our present findings provide evidence suggesting a role for an attenuated placental as well as fetal 11beta-HSD2 in the pathogenesis of IUGR. 18061258 2008
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype RGD Uteroplacental insufficiency alters nephrogenesis and downregulates cyclooxygenase-2 expression in a model of IUGR with adult-onset hypertension. 17272666 2007
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype BEFREE This suggests that the reduced placental 11beta-HSD2 in FGR is not due to intrinsic abnormalities in trophoblast cells, but likely a result of extrinsic factors associated with FGR. 16271275 2006
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype BEFREE No mutations were found in the 11beta-HSD2 gene in the intrauterine growth restriction cohort, and imprinting analysis revealed that the 11beta-HSD2 gene was not imprinted. 11600574 2001
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.400 Biomarker phenotype HPO