Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis 		93 45 72 0.69 42 0.65
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		254 56 43 0.15 16 0.16
CUI: C0282193
Disease: Iron Overload
Iron Overload 		241 53 40 0.14 21 0.22
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 39 11 0.11 6 6.3E-02
CUI: C0039730
Disease: Thalassemia
Thalassemia 		136 18 21 0.11 2 2.6E-02
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 4 10 0.10 2 3.1E-02
CUI: C0037061
Disease: Siderosis
Siderosis 		23 2 9 9.3E-02 2 3.2E-02
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		179 13 22 9.2E-02 4 5.6E-02
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 8 8.9E-02 3 4.8E-02
CUI: C0023891
Disease: Liver Cirrhosis, Alcoholic
Liver Cirrhosis, Alcoholic 		126 15 17 8.9E-02 1 1.3E-02
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency 		104 0 15 8.7E-02 0 0
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 8 8.2E-02 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 7 8.1E-02 3 4.8E-02
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		51 0 10 8.1E-02 0 0
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		83 21 12 7.8E-02 8 0.11
CUI: C0013221
Disease: Drug toxicity
Drug toxicity 		86 0 12 7.6E-02 0 0
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug 		87 0 12 7.6E-02 0 0
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		74 0 11 7.5E-02 0 0
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis 		18 8 7 7.4E-02 1 1.4E-02
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		36 0 8 7.2E-02 0 0
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		23 0 7 7.1E-02 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 6 7.1E-02 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 6 7.1E-02 0 0
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration 		146 0 15 7.0E-02 0 0
CUI: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer 		102 0 12 6.9E-02 0 0