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 7.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 0.20
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
0 21 0 0 1 4.0E-02
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight
0 2 0 0 1 0.17
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 2 0.25
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
0 123 0 0 1 7.9E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome
0 144 0 0 2 1.4E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 0.20
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 8.3E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0 13 0 0 1 5.9E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
0 3 0 0 1 0.14
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 1 0.17
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 0.20
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 0.14
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 1 7.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 0.20
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 0.17
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 7.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 0.33
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.1E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 1 4.6E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 2.7E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 2.4E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess
96 0 1 7.9E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly
138 25 1 6.0E-03 1 3.4E-02