| Human Disease |
Opitz Gbbb Syndrome, Autosomal Dominant OMIM ID: 145410 |
| Synonyms | BBB Syndrome; Chromosome 22q11.2 Deletion Syndrome, Opitz Phenotype; G Syndrome; GBBB Syndrome; Hypertelorism with Esophageal Abnormality and Hypospadias; Hypertelorism-Hypospadias Syndrome; Hypospadias-Dysphagia Syndrome; Opitz Bbbg Syndrome; Opitz Gbbb Syndrome, Type II; Opitz Oculogenitolaryngeal Syndrome, Type II; Opitz-Frias Syndrome; Opitz-G Syndrome, Type II; OGS2; Telecanthus with Associated Abnormalities; Telecanthus-Hypospadias Syndrome |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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