beckwith-wiedemann syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. (Human Disease Ontology, DOID_5572)
External Link http://www.omim.org/entry/130650
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Genes

4 genes associated with the beckwith-wiedemann syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
H19 H19, imprinted maternally expressed transcript (non-protein coding)
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
NSD1 nuclear receptor binding SET domain protein 1