MeSH 搜索器

Beckwith-Wiedemann Syndrome

A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.
推出的年份: 1983
副标题
树号: C16.131.077.133, C16.131.260.080, C16.320.180.080
MeSH 单一 ID: D001506
进入的组:
  • Beckwith Wiedemann Syndrome
  • Syndrome, Beckwith-Wiedemann
  • Wiedemann Syndrome
  • Syndrome, Wiedemann
  • Wiedemann Syndromes
  • Wiedemann-Beckwith Syndrome
  • Syndrome, Wiedemann-Beckwith
  • Wiedemann Beckwith Syndrome
  • Wiedemann-Beckwith Syndrome (WBS)
  • Syndrome, Wiedemann-Beckwith (WBS)
  • Wiedemann Beckwith Syndrome (WBS)
  • Wiedemann-Beckwith Syndromes (WBS)
  • EMG Syndrome
  • EMG Syndromes
  • Syndrome, EMG
  • Exomphalos-Macroglossia-Gigantism Syndrome
  • Exomphalos Macroglossia Gigantism Syndrome
  • Exomphalos-Macroglossia-Gigantism Syndromes
  • Syndrome, Exomphalos-Macroglossia-Gigantism
早前的内容:
  • Abnormalities, Multiple (1968-1982)
  • Gigantism (1966-1982)
  • Hernia, Umbilical (1966-1982)
  • Macroglossia (1975-1982)
  • Tongue/abnormalities (1966-1974)

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