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: C0405581
Disease: Testicular dysfunction
Testicular dysfunction
13 0 3 9.7E-02 0 0
CUI: C2609247
Disease: Adrenal incidentaloma
Adrenal incidentaloma
13 0 3 9.7E-02 0 0
CUI: C1855520
Disease: Hyperglycemia, Postprandial
Hyperglycemia, Postprandial
37 0 5 9.4E-02 0 0
CUI: C2732979
Disease: Acquired long QT syndrome
Acquired long QT syndrome
14 0 3 9.4E-02 0 0
CUI: C4049636
Disease: ROSE Cluster 1
ROSE Cluster 1
14 0 3 9.4E-02 0 0
CUI: C1257963
Disease: Endogenous Hyperinsulinism
Endogenous Hyperinsulinism
26 0 4 9.3E-02 0 0
CUI: C1257964
Disease: Exogenous Hyperinsulinism
Exogenous Hyperinsulinism
26 0 4 9.3E-02 0 0
CUI: C1740794
Disease: Aortic wall hypertrophy
Aortic wall hypertrophy
3 0 2 9.1E-02 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic
15 0 3 9.1E-02 0 0
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
63 0 7 9.1E-02 0 0
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
63 0 7 9.1E-02 0 0
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2
63 0 7 9.1E-02 0 0
CUI: C3838754
Disease: Congenital leptin deficiency
Congenital leptin deficiency
3 0 2 9.1E-02 0 0
CUI: C0152066
Disease: Lobomycosis
Lobomycosis
16 0 3 8.8E-02 0 0
CUI: C0018200
Disease: Granuloma, Respiratory Tract
Granuloma, Respiratory Tract
4 0 2 8.7E-02 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele
4 0 2 8.7E-02 0 0
Renal Tubular Dysgenesis With Choanal Atresia And Athelia
4 0 2 8.7E-02 0 0
CUI: C2931758
Disease: Acquired angioedema
Acquired angioedema
4 0 2 8.7E-02 0 0
CUI: C0271680
Disease: Diabetic Polyneuropathies
Diabetic Polyneuropathies
42 0 5 8.6E-02 0 0
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight
42 0 5 8.6E-02 0 0
CUI: C0014733
Disease: Erysipelas
Erysipelas
17 0 3 8.6E-02 0 0
CUI: C1274648
Disease: Segmental vitiligo
Segmental vitiligo
17 0 3 8.6E-02 0 0
CUI: C1306762
Disease: Aortoiliac occlusive disease
Aortoiliac occlusive disease
17 0 3 8.6E-02 0 0
BESTROPHINOPATHY, AUTOSOMAL RECESSIVE
17 0 3 8.6E-02 0 0
CUI: C1257965
Disease: Compensatory Hyperinsulinemia
Compensatory Hyperinsulinemia
30 0 4 8.5E-02 0 0