Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hemochromatosis HFE disease C0018995 GeneticVariation 0.6 orphanet , disgenet
Hemochromatosis HFE disease C0018995 AlteredExpression 0.6 orphanet , disgenet
Hemochromatosis HFE disease C0018995 Biomarker 0.6 orphanet , disgenet
Hemochromatosis HAMP disease C0018995 GeneticVariation 0.4 disgenet
Hemochromatosis HJV disease C0018995 GeneticVariation 0.4 disgenet
Hemochromatosis SLC40A1 disease C0018995 Biomarker 0.4 disgenet
Hemochromatosis HJV disease C0018995 AlteredExpression 0.4 disgenet
Hemochromatosis HJV disease C0018995 Biomarker 0.4 disgenet
Hemochromatosis HAMP disease C0018995 AlteredExpression 0.4 disgenet
Hemochromatosis HAMP disease C0018995 Biomarker 0.4 disgenet
Hemochromatosis SLC40A1 disease C0018995 GeneticVariation 0.4 disgenet
Hemochromatosis TFR2 disease C0018995 AlteredExpression 0.4 disgenet
Hemochromatosis TFR2 disease C0018995 GeneticVariation 0.4 disgenet
Hemochromatosis TFR2 disease C0018995 Biomarker 0.4 disgenet
Hemochromatosis SLC40A1 disease C0018995 AlteredExpression 0.4 disgenet
Hemochromatosis TNF disease C0018995 Biomarker 0.35 disgenet
Hemochromatosis TNF disease C0018995 GeneticVariation 0.35 disgenet
Hemochromatosis BMP6 disease C0018995 Biomarker 0.35 disgenet
Hemochromatosis SLC11A2 disease C0018995 Biomarker 0.35 disgenet
Hemochromatosis BMP6 disease C0018995 GeneticVariation 0.35 disgenet
Hemochromatosis SLC11A2 disease C0018995 AlteredExpression 0.35 disgenet
Hemochromatosis SLC11A2 disease C0018995 GeneticVariation 0.35 disgenet
Hemochromatosis TNF disease C0018995 AlteredExpression 0.35 disgenet
Hemochromatosis CP disease C0018995 Biomarker 0.32 disgenet
Hemochromatosis CP disease C0018995 AlteredExpression 0.32 disgenet
Hemochromatosis CP disease C0018995 GeneticVariation 0.32 disgenet
Hemochromatosis HP disease C0018995 GeneticVariation 0.32 disgenet
Hemochromatosis HP disease C0018995 Biomarker 0.32 disgenet
Hemochromatosis BMP2 disease C0018995 Biomarker 0.31 disgenet
Hemochromatosis AKR1D1 disease C0018995 Biomarker 0.3 disgenet
Hemochromatosis B2M disease C0018995 GeneticVariation 0.22 disgenet
Hemochromatosis B2M disease C0018995 Biomarker 0.22 disgenet
Hemochromatosis HMOX1 disease C0018995 Biomarker 0.2 disgenet
Hemochromatosis ALAD disease C0018995 Therapeutic 0.2 disgenet
Hemochromatosis HLA-H disease C0018995 GeneticVariation 0.1 disgenet
Hemochromatosis HLA-H disease C0018995 Biomarker 0.1 disgenet
Hemochromatosis TFRC disease C0018995 Biomarker 0.1 disgenet
Hemochromatosis HLA-A disease C0018995 GeneticVariation 0.1 disgenet
Hemochromatosis HLA-A disease C0018995 Biomarker 0.1 disgenet
Hemochromatosis TFRC disease C0018995 AlteredExpression 0.1 disgenet
Hemochromatosis TFRC disease C0018995 GeneticVariation 0.1 disgenet
Hemochromatosis CYBRD1 disease C0018995 AlteredExpression 0.05 disgenet
Hemochromatosis CYBRD1 disease C0018995 GeneticVariation 0.05 disgenet
Hemochromatosis FTL disease C0018995 GeneticVariation 0.05 disgenet
Hemochromatosis TMPRSS6 disease C0018995 Biomarker 0.04 disgenet
Hemochromatosis HLA-B disease C0018995 GeneticVariation 0.04 disgenet
Hemochromatosis TMPRSS6 disease C0018995 GeneticVariation 0.04 disgenet
Hemochromatosis APOE disease C0018995 GeneticVariation 0.03 disgenet
Hemochromatosis TF disease C0018995 GeneticVariation 0.03 disgenet
Hemochromatosis UBE2D1 disease C0018995 AlteredExpression 0.03 disgenet
Hemochromatosis F5 disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis ACO1 disease C0018995 AlteredExpression 0.02 disgenet
Hemochromatosis TLR4 disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis ACO1 disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis FTH1 disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis SUCNR1 disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis EPO disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis COX8A disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis TIMP1 disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis MMP2 disease C0018995 Biomarker 0.02 disgenet
Hemochromatosis HEPH disease C0018995 AlteredExpression 0.02 disgenet
Hemochromatosis FTH1 disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis GNPAT disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis SUCNR1 disease C0018995 AlteredExpression 0.02 disgenet
Hemochromatosis COX8A disease C0018995 GeneticVariation 0.02 disgenet
Hemochromatosis PGF disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis IGHG3 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis GNRH1 disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis CFTR disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis TP53 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis ALB disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis SHBG disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis GABPA disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis GDF15 disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis TRIM31 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis PCSK7 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis HLA-F disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis MCIDAS disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis SOD2 disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis NUP42 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis FXN disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis GAPDH disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis NMBR disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis FOXC2 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis CTNNB1 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis IL6 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis MMP3 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis IGFALS disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis UROD disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis SOD1 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis CYLD disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis NFE2L2 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis BTBD9 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis CCL2 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis MDM2 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis IREB2 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis CALR disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis IFNG disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis SMAD1 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis LINC01194 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis CD68 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis GPT disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis CELP disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis UBL3 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis GAST disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis PIEZO1 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis MPO disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis MFT2 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis ZKSCAN8 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis ALAS2 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis ADIPOQ disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis PPP1R11 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis S100A9 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis SERPINA1 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis ARNTL disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis GSTP1 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis SMAD7 disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis TNMD disease C0018995 Biomarker 0.01 disgenet
Hemochromatosis ELANE disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis IL10 disease C0018995 AlteredExpression 0.01 disgenet
Hemochromatosis ALDH2 disease C0018995 GeneticVariation 0.01 disgenet
Hemochromatosis SLC46A1 disease C0018995 GeneticVariation 0.01 disgenet
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