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: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome
0 7 0 0 2 0.12
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 5.3E-02
CUI: C0021845
Disease: Intestinal Perforation
Intestinal Perforation
0 3 0 0 1 7.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 9.1E-02
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
0 18 0 0 1 3.6E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum
0 35 0 0 2 4.5E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer
0 2 0 0 1 8.3E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 2 0.14
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
0 9 0 0 1 5.3E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 9.1E-02
CUI: C0424101
Disease: Inattention
Inattention
0 22 0 0 1 3.1E-02
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder)
0 37 0 0 1 2.1E-02
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy
0 12 0 0 1 4.5E-02
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia
0 1 0 0 1 9.1E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 6.7E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0 13 0 0 1 4.3E-02
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
0 24 0 0 1 2.9E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
0 3 0 0 1 7.7E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 2 0.18
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 9.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 7.7E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 2 0.11
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 9.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 5.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 3 0.27