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: C4021971
Disease: Peripheral arteriovenous fistula
Peripheral arteriovenous fistula 		8 0 5 9.3E-02 0 0
CUI: C2873756
Disease: Severe beta thalassemia
Severe beta thalassemia 		9 0 5 9.1E-02 0 0
CUI: C0271980
Disease: beta^0^ Thalassemia
beta^0^ Thalassemia 		34 0 7 9.0E-02 0 0
CUI: C0282193
Disease: Iron Overload
Iron Overload 		241 53 24 9.0E-02 4 4.7E-02
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 5 8.9E-02 0 0
CUI: C0039730
Disease: Thalassemia
Thalassemia 		136 0 15 8.7E-02 0 0
CUI: C0037054
Disease: Sickle Cell Trait
Sickle Cell Trait 		75 0 10 8.6E-02 0 0
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia 		92 0 11 8.3E-02 0 0
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies 		80 0 10 8.3E-02 0 0
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		83 0 10 8.1E-02 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 0 6 8.0E-02 0 0
CUI: C4021977
Disease: Visceral angiomatosis
Visceral angiomatosis 		17 0 5 7.9E-02 0 0
CUI: C0271987
Disease: ^A^gamma delta beta^0^ thalassemia
^A^gamma delta beta^0^ thalassemia 		4 0 4 7.8E-02 0 0
CUI: C0472777
Disease: Hemoglobin E/beta thalassemia disease
Hemoglobin E/beta thalassemia disease 		4 0 4 7.8E-02 0 0
CUI: C2673913
Disease: Anemia, Hypochromic Microcytic, With Iron Overload
Anemia, Hypochromic Microcytic, With Iron Overload 		4 2 4 7.8E-02 2 5.6E-02
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 4 7.8E-02 0 0
CUI: C4023136
Disease: Reduced alpha/beta synthesis ratio
Reduced alpha/beta synthesis ratio 		4 0 4 7.8E-02 0 0
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia 		156 44 15 7.8E-02 1 1.3E-02
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		144 0 14 7.7E-02 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		33 0 6 7.7E-02 0 0
CUI: C4274391
Disease: Dominant beta-thalassemia
Dominant beta-thalassemia 		5 0 4 7.7E-02 0 0
CUI: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume 		6 0 4 7.5E-02 0 0
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		35 0 6 7.5E-02 0 0
CUI: C3149631
Disease: MELORHEOSTOSIS, ISOLATED
MELORHEOSTOSIS, ISOLATED 		35 0 6 7.5E-02 0 0
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous 		36 0 6 7.4E-02 0 0