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: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis 		53 6 30 0.16 6 0.29
CUI: C0349459
Disease: Cervical intraepithelial neoplasia grade 2
Cervical intraepithelial neoplasia grade 2 		77 3 8 3.5E-02 3 0.14
CUI: C0024620
Disease: Primary Malignant Liver Neoplasm
Primary Malignant Liver Neoplasm 		60 4 10 4.7E-02 3 0.14
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		12 5 5 3.0E-02 3 0.13
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency 		70 8 10 4.5E-02 3 0.12
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 11 2 1.1E-02 3 0.10
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 2 16 7.5E-02 2 9.5E-02
CUI: C0221165
Disease: Diplegia
Diplegia 		4 2 2 1.2E-02 2 9.5E-02
CUI: C0746731
Disease: Acute myocardial ischemia
Acute myocardial ischemia 		32 2 3 1.6E-02 2 9.5E-02
CUI: C1332221
Disease: Adult Yolk Sac Tumor
Adult Yolk Sac Tumor 		35 2 12 6.5E-02 2 9.5E-02
CUI: C3826044
Disease: Lymphoblastic leukemia in children
Lymphoblastic leukemia in children 		19 2 4 2.3E-02 2 9.5E-02
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 3 2 1.1E-02 2 9.1E-02
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		47 3 5 2.5E-02 2 9.1E-02
CUI: C0677949
Disease: Stage III Colorectal Cancer
Stage III Colorectal Cancer 		45 3 6 3.0E-02 2 9.1E-02
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		115 15 12 4.5E-02 3 9.1E-02
CUI: C3146250
Disease: Stage III Colorectal Cancer AJCC v7
Stage III Colorectal Cancer AJCC v7 		44 3 6 3.0E-02 2 9.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		1 3 1 6.2E-03 2 9.1E-02
CUI: C0280803
Disease: Primary central nervous system lymphoma
Primary central nervous system lymphoma 		156 4 8 2.6E-02 2 8.7E-02
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		5 4 1 6.0E-03 2 8.7E-02
CUI: C0221166
Disease: Paraparesis
Paraparesis 		31 5 1 5.2E-03 2 8.3E-02
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		25 5 1 5.4E-03 2 8.3E-02
CUI: C0432470
Disease: 46, XY female
46, XY female 		25 5 12 6.9E-02 2 8.3E-02
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 3 1.6E-02 2 8.3E-02
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 5 1 6.1E-03 2 8.3E-02
CUI: C0220810
Disease: Congenital defects
Congenital defects 		126 6 14 5.1E-02 2 8.0E-02