CRYAB, crystallin alpha B, 1410

N. diseases: 200; N. variants: 30
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract
0.200 Biomarker disease MGD p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract. 23872361 2013