Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C0086543
Disease: Cataract
Cataract 		0.700 GeneticVariation LHGDN Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8. 17724170

2007
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C0086543
Disease: Cataract
Cataract 		0.700 GeneticVariation LHGDN "A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant ""coral-like"" cataract linked to chromosome 2q." 15041957

2004
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C0086543
Disease: Cataract
Cataract 		0.700 Biomarker LHGDN The P23T cataract mutation causes loss of solubility of folded gammaD-crystallin. 15451671

2004
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD
CUI: C0086543
Disease: Cataract
Cataract 		0.700 GeneticVariation LHGDN Sequencing of the coding regions of the CRYGA, B, C, and D genes showed the presence of a heterozygous C>A transversion in exon 2 of CRYGD that is associated with cataracts in this family. 12676897

2003