Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Embryonal nuclear cataract (disorder)
0.020 GeneticVariation disease BEFREE Identification of a novel GJA3 mutation in congenital nuclear cataract. 25635993 2015
Embryonal nuclear cataract (disorder)
0.020 GeneticVariation disease BEFREE A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. 21552498 2011