PRDX2, peroxiredoxin 2, 7001

N. diseases: 243; N. variants: 2
Disease: Creutzfeldt-Jakob Disease, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Familial 		0.010 GeneticVariation disease BEFREE A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease. 1357594 1992