Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract
0.320 GermlineCausalMutation ORPHANET A Novel Insertion Variant of CRYGD Is Associated with Congenital Nuclear Cataract in a Chinese Family. 26147294

2015

Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract
0.320 GermlineCausalMutation ORPHANET Molecular genetics of congenital nuclear cataract. 24384146

2014

Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract
0.320 GermlineCausalMutation ORPHANET A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family. 21031598

2011