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

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