SLC40A1, solute carrier family 40 member 1, 30061

N. diseases: 101; N. variants: 31
Disease: Ceruloplasmin deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		0.300 Biomarker disease CTD_human Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin. 20655381 2010