Comprehensive, easy-to-understand information about this condition
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Beckwith-Wiedemann syndrome due to CDKN1C mutation
MONDO:0016476
Beckwith-Wiedemann syndrome due to 11p15 microdeletion
MONDO:0016477
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
MONDO:0016478
Beckwith-Wiedemann syndrome due to NSD1 mutation
MONDO:0016547
Beckwith-Wiedemann syndrome due to 11p15 microduplication
MONDO:0019875
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
MONDO:0019923