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: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE 		1 0 1 1.00 0 0
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE 		1 0 1 1.00 0 0
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE 		1 0 1 1.00 0 0
CUI: C4225610
Disease: TRANSFERRIN VARIANT D(CHI)
TRANSFERRIN VARIANT D(CHI) 		1 0 1 1.00 0 0
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia 		3 0 1 0.33 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 0.17 0 0
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 0 1 0.17 0 0
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 0 1 0.17 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 1 1.0E-01 0 0
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 0 1 8.3E-02 0 0
CUI: C0428578
Disease: Iron level result
Iron level result 		12 0 1 8.3E-02 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas 		13 0 1 7.7E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 1 6.7E-02 0 0
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia 		16 0 1 6.2E-02 0 0
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 0 1 5.9E-02 0 0
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 0 1 5.0E-02 0 0
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 0 1 5.0E-02 0 0
CUI: C0013502
Disease: Echinococcosis
Echinococcosis 		21 0 1 4.8E-02 0 0
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		23 0 1 4.3E-02 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 4.2E-02 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 0 1 4.0E-02 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 0 1 3.8E-02 0 0
CUI: C4553297
Disease: Cystic Echinocccosis
Cystic Echinocccosis 		26 0 1 3.8E-02 0 0
CUI: C0483368
Disease: Human anaplasmosis due to Anaplasma phagocytophilum
Human anaplasmosis due to Anaplasma phagocytophilum 		29 0 1 3.4E-02 0 0
CUI: C0149519
Disease: Chronic Persistent Hepatitis
Chronic Persistent Hepatitis 		33 0 1 3.0E-02 0 0