CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266539
Disease: Congenital total cataract
Congenital total cataract
0.300 GermlineCausalMutation disease ORPHANET Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. 16862070 2006