Beckwith-Wiedemann syndrome

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:5572 - Beckwith-Wiedemann syndrome

Disease Ontology Definition:A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: igf2, nsd1, kcnq1, cdkn1c

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007534 - Beckwith-Wiedemann syndrome

MONDO:0007534 - Beckwith-Wiedemann syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndrome (is_a)