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Human Disease and Mouse Model Detail
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| Human Disease | Term: Opitz Gbbb Syndrome, Autosomal Dominant |
| Synonyms | BBB Syndrome; Chromosome 22q11.2 Deletion Syndrome, Opitz Phenotype; GBBB Syndrome; G Syndrome; Hypertelorism-Hypospadias Syndrome; Hypertelorism with Esophageal Abnormality and Hypospadias; Hypospadias-Dysphagia Syndrome; Opitz Bbbg Syndrome; Opitz-Frias Syndrome; Opitz Gbbb Syndrome, Type II; Opitz-G Syndrome, Type II; OGS2; Opitz Oculogenitolaryngeal Syndrome, Type II; Telecanthus-Hypospadias Syndrome; Telecanthus with Associated Abnormalities |
| Associated Genes |
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 04/03/2013 MGI 5.12 |
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