All diseases

OMIM ID
194050
OMIM term:
WILLIAMS-BEUREN SYNDROME; WBS
Alternative terms:
CHROMOSOME 7q11.23 DELETION SYNDROME, 1.5- TO 1.8-MB
WILLIAMS SYNDROME; WMS; WS
(∗) Location:
7q11.23  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Baz1b   Clip2   Dlg4   Eif4h   Fzd9   Gtf2i   Gtf2ird1   Limk1  

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* quick link - http://q.sanger.ac.uk/j0ld27gn