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 2.4E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 3.0E-02
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement
0 6 0 0 1 2.6E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 1 2.9E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 3.0E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.9E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 1 2.4E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.0E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 2.9E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 5.9E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 5.0E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 5.0E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
28 0 1 4.5E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 4.0E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 4.6E-03 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 0 1 4.8E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 4.9E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 1 4.9E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma
21 0 1 4.6E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 4.9E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 4.9E-03 0 0
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases
3 0 1 5.0E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 4.9E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 4.7E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 4.9E-03 0 0