EN2, engrailed homeobox 2, 2020

N. diseases: 41; N. variants: 8
Disease: Retinal defect ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0154823
Disease: Retinal defect
Retinal defect 		0.010 GeneticVariation phenotype BEFREE Retinal defects in mice lacking the autism-associated gene Engrailed-2. 30980901 2019