All diseases

OMIM ID
113620
OMIM term:
BRANCHIOOCULOFACIAL SYNDROME; BOFS
Alternative terms:
BOF SYNDROME
BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES, GROWTH RETARDATION, IMPERFORATE NASOLACRIMAL DUCT, AND PREMATURE AGING
HEMANGIOMATOUS BRANCHIAL CLEFTS-LIP PSEUDOCLEFT SYNDROME
LIP PSEUDOCLEFT-HEMANGIOMATOUS BRANCHIAL CYST SYNDROME
(∗) Location:
6p24.3  
(†) Associated OMIM genes:
TFAP2A  
(‡) Associated MGI genes:

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