CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Disease: CATARACT, MARNER TYPE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861821
Disease: CATARACT, MARNER TYPE
CATARACT, MARNER TYPE 		0.010 GeneticVariation disease BEFREE A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract. 25729975 2015