Source: ALL
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: C0016781
Disease: Fuchs Endothelial Dystrophy
Fuchs Endothelial Dystrophy 		0 32 0 0 1 2.4E-02
CUI: C0021845
Disease: Intestinal Perforation
Intestinal Perforation 		0 3 0 0 1 8.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.0E-01
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		0 18 0 0 1 3.7E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		0 21 0 0 1 3.3E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer 		0 2 0 0 1 9.1E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.6E-03
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder 		0 9 0 0 1 5.6E-02
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0 226 0 0 1 4.3E-03
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 4.5E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 8.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.0E-01
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.0E-01
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 9.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 5.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 8.3E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		620 0 1 1.5E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 1 1.6E-03 0 0
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		545 0 1 1.7E-03 0 0
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders 		535 0 1 1.7E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 1 1.8E-03 0 0
CUI: C0007124
Disease: Noninfiltrating Intraductal Carcinoma
Noninfiltrating Intraductal Carcinoma 		486 0 1 1.8E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 1 2.0E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height 		1903 0 4 2.0E-03 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		420 0 1 2.1E-03 0 0