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

Preferred term

Beckwith-Wiedemann Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

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

Scope note

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

History note

  • 1983

In other languages

  • Beckwith-Wiedemannin oireyhtymä

    Finnish

  • Beckwith
  • Beckwith-Wiedemann
  • Beckwith-Wiedemannin syndrooma
  • Beckwith-Wiedemannin tauti
  • eksomfalos-makroglossia-gigantismi-oireyhtymä
  • eksomfalos-makroglossia-gigantismi-syndrooma
  • EMG-oireyhtymä
  • EMG-syndrooma
  • morbus Beckwith-Wiedemann
  • syndroma Beckwith-Wiedemann
  • Wiedemann
  • Beckwith-Wiedemanns syndrom

    Swedish

  • BWS
  • EMG syndrom

URI

http://www.yso.fi/onto/mesh/D001506

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