PEG10, paternally expressed 10, 23089

N. diseases: 75; N. variants: 1
Disease: Fetal Growth Retardation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.020 AlteredExpression phenotype BEFREE Therefore, our results suggest that changes of the DNA methylation levels of the promoter regions and the expression patterns of Cdkn1c and Peg10 may be involved in the etiology of Cd-induced fetal growth restriction. 28823913 2017
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.020 GeneticVariation phenotype BEFREE Prenatal growth retardation identified in the patient may be due to deletion of the paternal allele of the PEG10 gene. 18651096 2008