Disease: Cataract ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cataract
CUI: C0086543
Disease: Cataract
0.010 GeneticVariation BEFREE The R36S mutation in CRYGD identified in this Chinese family caused a nuclear golden crystal cataract phenotype not described before. 16288201 2005