All diseases

OMIM ID
106260
OMIM term:
ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE
Alternative terms:
AEC SYNDROME
HAY-WELLS SYNDROME
(∗) Location:
3q28  
(†) Associated OMIM genes:
TP63  
(‡) Associated MGI genes:

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