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Beckwith-Wiedemann Syndrome (MONDO:0007534)

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations.

Overview

Category

Ontology ID

Internal:8915

Synonyms

BWS

Beckwith-Wiedemann syndrome

Wiedemann-Beckwith syndrome

exomphalos-macroglossia-gigantism syndrome

Beckwith-Wiedemann syndrome chromosome region

EMG syndrome

Wiedemann-Beckwith syndrome (WBS)

exomphalos macroglossia gigantism syndrome

Mapped terms

DOID:5572

GARD:0003343

ICD9:759.89

MEDGEN:2562

MESH:D001506

MedDRA:10050344

NANDO:2200959

NCIT:C34415

NORD:845

OMIM:130650

Orphanet:116

SCTID:81780002

UMLS:C0004903

icd11.foundation:803086260

Child terms