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: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0 7 0 0 1 5.0E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 4.5E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 7.1E-02
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0 68 0 0 2 2.5E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		0 21 0 0 1 2.9E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 5.6E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.4E-03
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0 12 0 0 1 4.0E-02
CUI: C0919890
Disease: Hyperfibrinogenemia
Hyperfibrinogenemia 		0 1 0 0 1 7.1E-02
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0 19 0 0 1 3.1E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 1 2.9E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 3.8E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 6.2E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 7.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 7.1E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 6.7E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 4.5E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 6.2E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 1 1.1E-03 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		656 0 1 1.4E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 1 1.4E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		610 0 1 1.5E-03 0 0
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		462 79 1 1.9E-03 1 1.1E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		430 0 1 2.0E-03 0 0
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma 		420 0 1 2.0E-03 0 0