All diseases

OMIM ID
300000
OMIM term:
OPITZ GBBB SYNDROME, X-LINKED
Alternative terms:
OPITZ GBBB SYNDROME, TYPE I; GGGB1
OPITZ SYNDROME; OS
OPITZ SYNDROME, X-LINKED; OSX
OPITZ-G SYNDROME, TYPE I; OGS1
OPITZ BBBG SYNDROME, TYPE I; BBBG1
HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS
HYPERTELORISM-HYPOSPADIAS SYNDROME
TELECANTHUS-HYPOSPADIAS SYNDROME
(∗) Location:
Xp22.2  
(†) Associated OMIM genes:
MID1  
(‡) Associated MGI genes:
Mid1  

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