CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Disease: Corneal Opacity ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		0.110 GeneticVariation phenotype LHGDN Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA). 18302245 2008
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		0.110 Biomarker phenotype HPO