Gene: NYX ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60506
Gene Symbol: NYX
NYX 		0.130 GeneticVariation disease BEFREE Myopia is a complex eye disorder.The X-linked form of complete congenital stationary night blindness (CSNB1A) is usually associated with moderate to high myopia, and is caused by mutations in the NYX gene. 23406521 2013
Entrez Id: 60506
Gene Symbol: NYX
NYX 		0.130 Biomarker disease BEFREE The observations suggest that NYX may have independent effects on myopia and night blindness. 17392683 2007
Entrez Id: 60506
Gene Symbol: NYX
NYX 		0.130 GeneticVariation disease LHGDN Mutations in NYX of individuals with high myopia, but without night blindness. 17392683 2007
Entrez Id: 60506
Gene Symbol: NYX
NYX 		0.130 GeneticVariation disease BEFREE The importance of associated myopia with NYX mutations is discussed. 16670814 2006
Entrez Id: 60506
Gene Symbol: NYX
NYX 		0.130 Biomarker disease HPO