CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Hereditary hemochromatosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		0.320 Biomarker disease CTD_human To evaluate whether Cp might act as a modifier gene of genetic hemochromatosis, we intercrossed C3H Hfe(-/-) and C3HDiSnA Cp(R435X/R435X) mice. 17258727 2007
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		0.320 GeneticVariation disease BEFREE The present study investigated the serum levels of Cp and its ferroxidase activity in 53 C282Y homozygote genetic hemochromatosis (38 iron overloaded, 15 iron depleted) patients as compared to age and sex-matched healthy volunteers. 11804665 2002
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		0.320 AlteredExpression disease BEFREE Reduced serum ceruloplasmin levels in hereditary haemochromatosis. 11472372 2001