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: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms
0 2 0 0 1 1.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.1E-02
Infections specific to perinatal period
0 1 0 0 1 1.1E-02
CUI: C0242453
Disease: Prostatism
Prostatism
0 1 0 0 1 1.1E-02
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis
0 9 0 0 1 1.0E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 1.0E-02
Non-small cell lung cancer stage III
0 1 0 0 1 1.1E-02
CUI: C0334279
Disease: Adenocarcinoma, intestinal type
Adenocarcinoma, intestinal type
0 2 0 0 1 1.1E-02
CUI: C0796003
Disease: Juberg-Marsidi syndrome
Juberg-Marsidi syndrome
0 14 0 0 1 9.7E-03
CUI: C0948698
Disease: Coronary spastic angina
Coronary spastic angina
0 1 0 0 1 1.1E-02
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
0 1 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 1.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.1E-02
Primary low grade serous adenocarcinoma of ovary
0 1 0 0 1 1.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.0E-02
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 3.2E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 3.2E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 3.2E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 3.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 3.3E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma
11 0 1 3.2E-03 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
9 0 1 3.3E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 3.3E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 3.3E-03 0 0