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: C0030922
Disease: Peptic Ulcer Hemorrhage
Peptic Ulcer Hemorrhage
2 0 1 0.14 0 0
CUI: C0040715
Disease: Chromosomal translocation
Chromosomal translocation
2 0 1 0.14 0 0
CUI: C0206629
Disease: Pulmonary Blastoma
Pulmonary Blastoma
10 0 2 0.14 0 0
CUI: C0266444
Disease: Congenital absence of vas deferens
Congenital absence of vas deferens
10 0 2 0.14 0 0
CUI: C0266807
Disease: Acute gastrointestinal hemorrhage
Acute gastrointestinal hemorrhage
2 0 1 0.14 0 0
CUI: C1333866
Disease: Grade 1 Colon Adenocarcinoma
Grade 1 Colon Adenocarcinoma
2 0 1 0.14 0 0
CUI: C1959584
Disease: Cardiac Carcinoma
Cardiac Carcinoma
10 0 2 0.14 0 0
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder)
10 0 2 0.14 0 0
CUI: C3203672
Disease: CYP2C19 polymorphism
CYP2C19 polymorphism
10 0 2 0.14 0 0
CUI: C3494186
Disease: Autosomal Hemophilia A
Autosomal Hemophilia A
2 0 1 0.14 0 0
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen
2 0 1 0.14 0 0
CUI: C4331269
Disease: Sacral Chordoma
Sacral Chordoma
10 0 2 0.14 0 0
CUI: C4551627
Disease: Granulocytopenic disorder
Granulocytopenic disorder
10 0 2 0.14 0 0
CUI: C0677483
Disease: Carcinoma testes
Carcinoma testes
11 0 2 0.13 0 0
CUI: C0042267
Disease: Vaginitis
Vaginitis
12 0 2 0.12 0 0
CUI: C0278719
Disease: Extraocular retinoblastoma
Extraocular retinoblastoma
3 0 1 0.12 0 0
Hyperthyroidism secondary to amiodarone
3 0 1 0.12 0 0
CUI: C1333855
Disease: Grade 3 Colon Adenocarcinoma
Grade 3 Colon Adenocarcinoma
3 0 1 0.12 0 0
CUI: C3826394
Disease: Epilepsy in children
Epilepsy in children
12 1 2 0.12 1 1.0E-01
CUI: C3899731
Disease: Calcineurin Nephrotoxicity
Calcineurin Nephrotoxicity
3 0 1 0.12 0 0
CUI: C4024702
Disease: Reduced factor X activity
Reduced factor X activity
3 0 1 0.12 0 0
CUI: C4284040
Disease: FIGO Stage III Ovarian Cancer
FIGO Stage III Ovarian Cancer
3 0 1 0.12 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B
13 0 2 0.12 0 0
CUI: C0496870
Disease: Benign neoplasm of liver
Benign neoplasm of liver
13 0 2 0.12 0 0
CUI: C1861502
Disease: COLCHICINE RESISTANCE
COLCHICINE RESISTANCE
13 3 2 0.12 1 8.3E-02