FTH1, ferritin heavy chain 1, 2495

N. diseases: 107; N. variants: 18
Disease: Hemochromatosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis 		0.020 GeneticVariation disease LHGDN A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin. 11783942 2003
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis 		0.020 Biomarker disease BEFREE Fine mapping of a human chromosome 6 ferritin heavy chain pseudogene: relevance to haemochromatosis. 1757092 1991