Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.010 GeneticVariation BEFREE Although this is an excellent candidate gene for hereditary retinopathies, single-strand conformation polymorphism analyses provided no evidence that variations in IMPG2 coding region are responsible for the inherited retinopathies examined. 11726612

2001