MID1
| Deellabo: | PGD DNA |
| Gen (Gen Code): | MID1 |
| Aliases Gen: | BBBG1, FXY, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY |
| Gen ID (NCBI): | 4281 |
| OMIM Gen ID: | 300552 |
| Chromosomale locatie: | Xp22 |
| Genetische aandoening / Analyse: | Opitz GBBB syndroom, X-gebonden |
| OMIM aandoening ID: | 300000 |
| Overerving: | X-linked R |
| Aliases aandoening: | OPITZ GBBB SYNDROME, X-LINKED 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 |