All diseases

OMIM ID
130650
OMIM term:
BECKWITH-WIEDEMANN SYNDROME; BWS
Alternative terms:
EXOMPHALOS-MACROGLOSSIA-GIGANTISM SYNDROME
EMG SYNDROME
WIEDEMANN-BECKWITH SYNDROME; WBS BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION, INCLUDED; BWCR, INCLUDED
(∗) Location:
11p15.4   11p15.5   5q35.2-q35.3  
(†) Associated OMIM genes:
CDKN1C   H19   KCNQ1OT1   NSD1  
(‡) Associated MGI genes:
Cdkn1c   Spnb2  

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