|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. (Human Disease Ontology, DOID_5572)|
|Downloads & Tools|
1 genes associated with the Beckwith-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|CDKN1C||cyclin-dependent kinase inhibitor 1C (p57, Kip2)|