CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C1801950 | Opitz-G syndrome, type 2 | DO | Opitz-GBBB syndrome | 0050780 |
C1801950 | Opitz-G syndrome, type 2 | MONDO | autosomal dominant Opitz G/BBB syndrome | 0007779 |
C1801950 | Opitz-G syndrome, type 2 | MONDO | Opitz G/BBB syndrome | 0017138 |
C1801950 | Opitz-G syndrome, type 2 | MSH | Hypertelorism with esophageal abnormality and hypospadias | C538387 |
C1801950 | Opitz-G syndrome, type 2 | MSH | Opitz-G syndrome, type 2 | C538387 |
C1801950 | Opitz-G syndrome, type 2 | NCI | Opitz G Syndrome | C125487 |
C1801950 | Opitz-G syndrome, type 2 | NCI | Opitz G/BBB Syndrome | C125487 |
C1801950 | Opitz-G syndrome, type 2 | OMIM | OPITZ-FRIAS SYNDROME | 145410 |
C1801950 | Opitz-G syndrome, type 2 | OMIM | OPITZ GBBB SYNDROME, TYPE II | 145410 |
C1801950 | Opitz-G syndrome, type 2 | ORDO | Opitz G/BBB syndrome | 2745 |
C1801950 | Opitz-G syndrome, type 2 | ORDO | Autosomal dominant Opitz G/BBB syndrome | 306588 |