CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Complement component 5 deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0343047
Disease: Complement component 5 deficiency
Complement component 5 deficiency 		0.010 GeneticVariation disease BEFREE Other marker systems excluded from linkage with C5 deficiency included the ceruloplasmin and Duffy loci at a recombination frequency of less than 15%, and the erythrocyte glyoxalase, MN, and Lewis loci at a recombination frequency of less than 5%. 886187 1977