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DeCS
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![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) ![](/decsserver/images/bar/pixel.gif) |
Descriptor English:
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Beckwith-Wiedemann Syndrome
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Descriptor Spanish:
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Síndrome de Beckwith-Wiedemann
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Descriptor Portuguese:
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Síndrome de Beckwith-Wiedemann
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Synonyms English:
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Exomphalos-Macroglossia-Gigantism Syndrome
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Tree Number:
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C16.131.077.133
C16.131.260.080
C16.320.180.080
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Definition English:
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A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities. |
Indexing Annotation English:
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a syndrome of multiple abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: EMG SYNDROME
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History Note English:
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83
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Allowable Qualifiers English:
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Record Number:
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1524
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Unique Identifier:
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D001506
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Occurrence in VHL:
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Similar:
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DeCS SciELO LILACS LIS
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