CRYGS, crystallin gamma S, 1427

N. diseases: 15; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3277059
Disease: Congenital Bilateral Cataracts
Congenital Bilateral Cataracts
0.010 GeneticVariation disease BEFREE We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin. 19262743 2009