Skip to main

Medical Subject Headings (thesaurus)

Search from vocabulary

mapear
anotar
descargar

Concept information

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

Término preferido

Beckwith-Wiedemann Syndrome  

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

Tipo

  • mesh:Descriptor

Definición

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

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

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

En otras lenguas

  • Syndrome de Beckwith-Wiedemann

    francés

  • 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

Descargue este concepto:

RDF/XML TURTLE JSON-LD Creado 26/4/82, última modificación 12/5/21