- OMIM ID
-
145410
- OMIM term:
- OPITZ GBBB SYNDROME, AUTOSOMAL DOMINANT
- Alternative terms:
-
OPITZ GBBB SYNDROME, TYPE II
HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS
G SYNDROME
HYPOSPADIAS-DYSPHAGIA SYNDROME
OPITZ-FRIAS SYNDROME
OPITZ-G SYNDROME, TYPE II; OGS2
TELECANTHUS WITH ASSOCIATED ABNORMALITIES
BBB SYNDROME
HYPERTELORISM-HYPOSPADIAS SYNDROME
TELECANTHUS-HYPOSPADIAS SYNDROME
OPITZ BBBG SYNDROME
GBBB SYNDROME
OPITZ OCULOGENITOLARYNGEAL SYNDROME, TYPE II
CHROMOSOME 22q11.2 DELETION SYNDROME, OPITZ PHENOTYPE
- (∗) Location:
- 22q11.2
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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