CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract
0.400 GermlineCausalMutation disease ORPHANET Molecular genetics of congenital nuclear cataract. 24384146 2014
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract
0.400 GermlineCausalMutation disease ORPHANET A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family. 18618005 2008
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract
0.400 Biomarker disease HPO