Related LncRNAs
ID	lncRNA Name	Disease	Method	Sample	Expression pattern	Dysfunction type	Description	PMID	Source
EL0556	H19	Silver-Russell syndrome	N/A	N/A	N/A	mutation	Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome	19066168	LncRNADisease
EL0556	H19	Silver-Russell syndrome	N/A	N/A	N/A	epigenetics	The major finding (~44%) is a hypomethylation of the imprinting control region 1 (ICR1) in 11p15.5 affecting the expression of H19 and IGF2. 4-10% of the patients carry a maternal UPD of chromosome 7 (UPD(7)mat).	21150838	LncRNADisease
EL0864	MESTIT1	Silver-Russell syndrome	N/A	N/A	N/A	N/A	Association	12746419	LncRNADisease