Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1420
Gene Symbol: CRYGC
CRYGC
CUI: C0086543
Disease: Cataract
Cataract 		0.460 GeneticVariation LHGDN The present study has identified a novel nonsense mutation in CRYGC associated with autosomal dominant cataracts and microcornea in a Chinese family. 19204787

2009
Entrez Id: 1420
Gene Symbol: CRYGC
CRYGC
CUI: C0086543
Disease: Cataract
Cataract 		0.460 GeneticVariation LHGDN A novel nonsense mutation in CRYGC was detected in a Chinese family with consistent autosomal dominant congenital nuclear cataract, providing clear evidence of a relationship between the genotype and the corresponding cataract phenotype. 18618005

2008