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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 7.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 0.17
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder
0 61 0 0 1 1.5E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 3 8.8E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
0 123 0 0 1 7.8E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 0.17
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma
0 4 0 0 3 0.43
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 8.0E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
0 3 0 0 1 0.12
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 0.17
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 0.12
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 0.17
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 0.14
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 7.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 0.29
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 7.6E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 1.4E-02 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 1.4E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 1.3E-02 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis
22 0 1 1.1E-02 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 1.3E-02 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
28 0 1 1.1E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 8.5E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 1.2E-02 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 1.5E-02 0 0