Gene: NR0B1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 190
Gene Symbol: NR0B1
NR0B1 		0.110 Biomarker disease BEFREE We report a girl with a de novo deletion at Xp21.2 on the maternal chromosome, including DAX1, the GK gene and 3' end of the dystrophin gene, who presented with salt losing adrenal insufficiency and moderate developmental delay, but relatively mild features of muscular dystrophy. 18762570 2008
Entrez Id: 190
Gene Symbol: NR0B1
NR0B1 		0.110 Biomarker disease HPO