Beckwith-Wiedemann syndrome BWS Beckwith-Wiedemann syndrome Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations. Beckwith-Wiedemann syndrome chromosome region DOID:5572 EMG syndrome GARD:0003343 ICD10:Q87.3 ICD9:759.89 MESH:D001506 MONDO:0007534 MedDRA:10050344 NCIT:C34415 OMIM:130650 Orphanet:116 SCTID:81780002 UMLS:C0004903 Wiedemann-Beckwith syndrome Wiedemann-Beckwith syndrome (WBS) exomphalos macroglossia gigantism syndrome exomphalos-macroglossia-gigantism syndrome https://rarediseases.info.nih.gov/diseases/3343/beckwith-wiedemann-syndrome macroglossia syndrome or malformation associated with head and neck malformations syndromic urogenital tract malformation polymalformative genetic syndrome with increased risk of developing cancer familial syndrome associated with hypertrophic cardiomyopathy inherited renal cancer-predisposing syndrome genetic otorhinolaryngologic disease overgrowth syndrome syndromic renal or urinary tract malformation hereditary connective tissue disorder