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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Chromosome Disorders > Beckwith-Wiedemann Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Chromosome Disorders > Beckwith-Wiedemann Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Beckwith-Wiedemann Syndrome

Preferred term

Beckwith-Wiedemann Syndrome  

Type

  • mesh:Descriptor

Definition

  • A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.

Broader concept

Related concepts

Entry terms

  • EMG Syndrome
  • Exomphalos-Macroglossia-Gigantism Syndrome
  • Wiedemann-Beckwith Syndrome
  • Wiedemann-Beckwith Syndrome (WBS)
  • Wiedemann Syndrome

Allowable Qualifier(s)

In other languages

  • Syndrome de Beckwith-Wiedemann

    French

  • Omphalocèle-macroglossie-gigantisme
  • SBW (Syndrome de Beckwith-Wiedemann)
  • SWB (Syndrome de Wiedemann-Beckwith)
  • Syndrome d'hypertrophie staturale avec macroglossie et omphalocèle
  • Syndrome de Wiedemann-Beckwith
  • Syndrome omphalocèle-macroglossie-gigantisme

URI

http://data.loterre.fr/ark:/67375/JVR-LLFZ7FD5-V

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RDF/XML TURTLE JSON-LD Created 4/26/82, last modified 5/12/21