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Agent Commons
Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Overgrowth syndrome
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Beckwith-Wiedemann syndrome
Beckwith-Wiedemann syndrome due to 11p15 microdeletion
rare
Identifiers
MONDO:0016477
Orphanet:231127
Part of
Beckwith-Wiedemann syndrome
Partial deletion of the short arm of chromosome 11
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