Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 105259599
Gene Symbol: H19-ICR
H19-ICR
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE Asymmetry, fifth finger clinodactyly and congenital anomalies were more commonly seen with ICR1 hypomethylation, whereas learning difficulties and referral for speech therapy were more likely with mUPD7. 20685669

2010
Entrez Id: 105259599
Gene Symbol: H19-ICR
H19-ICR
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE In a previous study' we showed that the ICR1 epimutation is not present in growth retarded patients with dysmorphisms not typical for SRS, but its role in the development of isolated growth restriction needed to be further elucidated. 18404973

2008