CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Disease: Cortical cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271160
Disease: Cortical cataract
Cortical cataract 		0.010 GeneticVariation disease BEFREE In 6 patients (4 patients with nuclear cataract and 2 with cortical cataract), sequence analysis of the exon 1 in the CRYAA gene showed a silent single nucleotide polymorphism [D2D] (CRYAA: C to T transition). 28146420 2017