Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		0.400 GermlineCausalMutation ORPHANET Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans. 23531866

2013