MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
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 		0.010 Biomarker disease BEFREE Lens-specific conditional knockout of Msx2 in mice leads to ocular anterior segment dysgenesis via activation of a calcium signaling pathway. 30683901 2019