PRDX3, peroxiredoxin 3, 10935

N. diseases: 89; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339282
Disease: Pre-descemet's corneal dystrophy
Pre-descemet's corneal dystrophy
0.010 GeneticVariation disease BEFREE The same PRDX3 variant was identified in the previously reported PPPCD family expressing the common PPPCD phenotype, and is predicted by in silico prediction tools to be damaging to protein function. 31782998 2020