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: C0001948
Disease: Alcohol consumption
Alcohol consumption
0 535 0 0 1 1.8E-03
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
0 4 0 0 1 7.1E-02
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia
0 11 0 0 2 1.0E-01
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0 220 0 0 1 4.3E-03
CUI: C0006060
Disease: Boutonneuse Fever
Boutonneuse Fever
0 3 0 0 1 7.7E-02
CUI: C0007859
Disease: Neck Pain
Neck Pain
0 3 0 0 1 7.7E-02
CUI: C0018862
Disease: Heberden node
Heberden node
0 1 0 0 1 9.1E-02
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis
0 2 0 0 1 8.3E-02
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism
0 7 0 0 2 0.12
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 9.1E-02
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor
0 1 0 0 1 9.1E-02
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria
0 24 0 0 1 2.9E-02
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder
0 2 0 0 1 8.3E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement
0 10 0 0 1 5.0E-02
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis
0 1 0 0 1 9.1E-02
CUI: C0264394
Disease: Paraseptal emphysema
Paraseptal emphysema
0 3 0 0 1 7.7E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
0 8 0 0 2 0.12
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
0 1 0 0 1 9.1E-02
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic
0 5 0 0 2 0.14
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis
0 8 0 0 1 5.6E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 9.1E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda
0 6 0 0 2 0.13
Secondary acquired sideroblastic anemia
0 2 0 0 2 0.18
CUI: C0337439
Disease: Iron measurement
Iron measurement
0 16 0 0 1 3.8E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome
0 4 0 0 1 7.1E-02