Genes
NR0B1
OMIMSynonym(s): DAX1, AHCH, AHC, DSS
Locus: Xp21.3
Protein: Nuclear receptor subfamily 0 group B member 1
Disorder(s):
- Isolated X-Linked Adrenal Hypoplasia Congenita
- Complex Glycerol Kinase Deficiency
- X-Linked Adrenal Hypoplasia Congenita
- NR0B1-Related 46,XY DSD and 46,XY CGD





