CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		0.300 Biomarker disease MGD Increased vulnerability to rotenone-induced neurotoxicity in ceruloplasmin-deficient mice. 18804145 2008
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		0.300 Biomarker disease MGD Copper transport and metabolism are normal in aceruloplasminemic mice. 11461924 2001
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		0.300 Biomarker disease MGD Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. 10485908 1999
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		0.300 CausalMutation disease CLINVAR