All diseases

OMIM ID
600920
OMIM term:
VAN DEN ENDE-GUPTA SYNDROME; VDEGS
Alternative terms:
MARDEN-WALKER-LIKE SYNDROME WITHOUT PSYCHOMOTOR RETARDATION
BLEPHAROPHIMOSIS, ARACHNODACTYLY, AND CONGENITAL CONTRACTURES
(∗) Location:
22q11.21  
(†) Associated OMIM genes:
SCARF2  
(‡) Associated MGI genes:

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