obsolete_Beckwith-Wiedemann syndrome https://rarediseases.info.nih.gov/diseases/3343/beckwith-wiedemann-syndrome true ICD9:759.89 Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations. Beckwith-Wiedemann syndrome MESH:D001506 Beckwith-Wiedemann syndrome chromosome region Wiedemann-Beckwith syndrome 3.41.0 BWS MedDRA:10050344 GARD:0003343 ICD10:Q87.3 Orphanet:116 exomphalos-macroglossia-gigantism syndrome SCTID:81780002 Replaced with Mondo term. http://purl.obolibrary.org/obo/MONDO_0007534 Wiedemann-Beckwith syndrome (WBS) UMLS:C0004903 DOID:5572 exomphalos macroglossia gigantism syndrome OMIM:130650 NCIT:C34415 EMG syndrome