CRYGS, crystallin gamma S, 1427

N. diseases: 15; N. variants: 5
Disease: Congenital lamellar cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract 		0.010 GeneticVariation disease BEFREE This included identification of: complex ocular phenotypes due to two novel PAX6 mutations; progressive cortical cataract and lamellar cataract with lens subluxation due to two novel CRYGS mutations. 28450710 2017