FOXD3, forkhead box D3, 27022

N. diseases: 78; N. variants: 4
Disease: Irido-corneal dysgenesis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266525
Disease: Irido-corneal dysgenesis
Irido-corneal dysgenesis 		0.310 Biomarker disease GENOMICS_ENGLAND FOXD3 variants increase the risk of anterior segment dysgenesis phenotypes in humans. 22815627 2012
CUI: C0266525
Disease: Irido-corneal dysgenesis
Irido-corneal dysgenesis 		0.310 GeneticVariation disease BEFREE FOXD3 variants increase the risk of anterior segment dysgenesis phenotypes in humans. 22815627 2012