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 6.7E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 5.9E-02
CUI: C0025202
Disease: melanoma
melanoma 		0 515 0 0 1 1.9E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.11
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0 61 0 0 1 1.4E-02
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0 68 0 0 1 1.3E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 35 0 0 1 2.3E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		0 21 0 0 1 3.4E-02
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		0 81 0 0 1 1.1E-02
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas 		0 138 0 0 1 6.8E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 7.7E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.6E-03
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		0 56 0 0 1 1.6E-02
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 144 0 0 1 6.6E-03
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0 12 0 0 1 5.0E-02
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0 19 0 0 1 3.7E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 1 3.4E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 4.8E-02
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome 		0 28 0 0 1 2.8E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 9.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.11
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.11
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 1.0E-01
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 5.9E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 9.1E-02