Beckwith-Wiedemann syndrome Gene Set

Dataset ClinVar Gene-Phenotype 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

1 genes associated with the Beckwith-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)