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: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 6 1.00 10 1.00
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 3 0.17 2 0.18
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 3 0.23 2 0.18
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		179 13 2 1.1E-02 3 0.15
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 3 0.15 4 0.13
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		83 21 3 3.5E-02 3 0.11
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 2 0.14 3 0.11
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 2 0.14 3 0.11
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 1.0E-01
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		6 1 1 9.1E-02 1 1.0E-01
CUI: C0333293
Disease: Healing ulcer
Healing ulcer 		43 1 1 2.1E-02 1 1.0E-01
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		5 1 1 1.0E-01 1 1.0E-01
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		3 1 1 0.12 1 1.0E-01
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 0.17 1 1.0E-01
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 0.17 1 1.0E-01
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 0.17 1 1.0E-01
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 3 0.10 4 9.5E-02
CUI: C0002894
Disease: Refractory anaemia with excess blasts
Refractory anaemia with excess blasts 		0 2 0 0 1 9.1E-02
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		37 2 1 2.4E-02 1 9.1E-02
CUI: C0037061
Disease: Siderosis
Siderosis 		23 2 1 3.6E-02 1 9.1E-02
CUI: C0042344
Disease: Varicose Ulcer
Varicose Ulcer 		38 2 1 2.3E-02 1 9.1E-02
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder 		10 2 1 6.7E-02 1 9.1E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		6 2 1 9.1E-02 1 9.1E-02
CUI: C0524988
Disease: Schnitzler Syndrome
Schnitzler Syndrome 		14 2 1 5.3E-02 1 9.1E-02
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 1 9.1E-02