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: C0220810
Disease: Congenital defects
Congenital defects
126 6 7 3.0E-02 3 0.21
CUI: C1096293
Disease: Macroangiopathy
Macroangiopathy
31 6 12 9.0E-02 3 0.21
CUI: C0403447
Disease: Chronic Kidney Insufficiency
Chronic Kidney Insufficiency
52 12 7 4.4E-02 4 0.21
CUI: C0035067
Disease: Renal Artery Stenosis
Renal Artery Stenosis
37 8 7 4.9E-02 3 0.19
CUI: C0747845
Disease: early pregnancy
early pregnancy
273 8 21 5.7E-02 3 0.19
Refractory anaemia with excess blasts
49 2 3 1.9E-02 2 0.18
CUI: C0037061
Disease: Siderosis
Siderosis
23 2 2 1.5E-02 2 0.18
CUI: C0221165
Disease: Diplegia
Diplegia
4 2 3 2.6E-02 2 0.18
Secondary acquired sideroblastic anemia
6 2 1 8.4E-03 2 0.18
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
10 2 1 8.1E-03 2 0.18
CUI: C0746731
Disease: Acute myocardial ischemia
Acute myocardial ischemia
32 2 5 3.5E-02 2 0.18
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis
12 2 4 3.3E-02 2 0.18
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
4 2 1 8.5E-03 2 0.18
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 2 0.18
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
1 2 1 8.8E-03 2 0.18
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
1 2 1 8.8E-03 2 0.18
CUI: C3826044
Disease: Lymphoblastic leukemia in children
Lymphoblastic leukemia in children
19 2 3 2.3E-02 2 0.18
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
15 3 1 7.8E-03 2 0.17
CUI: C0042341
Disease: Varicocele
Varicocele
99 3 14 7.0E-02 2 0.17
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic
15 3 5 4.0E-02 2 0.17
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction
47 3 12 8.1E-02 2 0.17
Cervical intraepithelial neoplasia grade 2
77 3 7 3.8E-02 2 0.17
Refractory anemia with ringed sideroblasts
36 3 3 2.0E-02 2 0.17
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda
4 3 1 8.5E-03 2 0.17
HFE-Associated Hereditary Hemochromatosis
10 3 1 8.1E-03 2 0.17