Gene: PXDN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7837
Gene Symbol: PXDN
PXDN 		0.020 GeneticVariation disease BEFREE PXDN mutations lead to severe eye disorders, including microphthalmia, cataract, glaucoma, and anterior segment dysgenesis in humans and mice. 31817535 2019
Entrez Id: 7837
Gene Symbol: PXDN
PXDN 		0.020 Biomarker disease BEFREE We conclude that PXDN sequencing should be considered in microphthalmia with anterior segment dysgenesis. 24939590 2015