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: C0221165
Disease: Diplegia
Diplegia 		4 2 1 1.1E-02 2 9.1E-02
CUI: C0746731
Disease: Acute myocardial ischemia
Acute myocardial ischemia 		32 2 5 4.2E-02 2 9.1E-02
CUI: C3826044
Disease: Lymphoblastic leukemia in children
Lymphoblastic leukemia in children 		19 2 2 1.9E-02 2 9.1E-02
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 3 1 9.5E-03 2 8.7E-02
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		47 3 1 7.3E-03 2 8.7E-02
CUI: C0349459
Disease: Cervical intraepithelial neoplasia grade 2
Cervical intraepithelial neoplasia grade 2 		77 3 2 1.2E-02 2 8.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 8.7E-02
CUI: C0024620
Disease: Primary Malignant Liver Neoplasm
Primary Malignant Liver Neoplasm 		60 4 2 1.3E-02 2 8.3E-02
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		5 4 1 1.1E-02 2 8.3E-02
CUI: C0221166
Disease: Paraparesis
Paraparesis 		31 5 1 8.3E-03 2 8.0E-02
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		25 5 1 8.7E-03 2 8.0E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 8.0E-02
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 1 8.8E-03 2 8.0E-02
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 5 1 1.1E-02 2 8.0E-02
CUI: C0220810
Disease: Congenital defects
Congenital defects 		126 6 5 2.4E-02 2 7.7E-02
CUI: C0268074
Disease: Indian childhood cirrhosis
Indian childhood cirrhosis 		67 6 2 1.3E-02 2 7.7E-02
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 2 1.8E-02 2 7.7E-02
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0 7 0 0 2 7.4E-02
CUI: C0278484
Disease: Malignant neoplasm of colon stage IV
Malignant neoplasm of colon stage IV 		108 7 8 4.2E-02 2 7.4E-02
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency 		70 8 2 1.3E-02 2 7.1E-02
CUI: C0747845
Disease: early pregnancy
early pregnancy 		273 8 15 4.3E-02 2 7.1E-02
CUI: C0004509
Disease: Azoospermia
Azoospermia 		254 70 31 9.9E-02 6 7.0E-02
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		188 9 6 2.2E-02 2 6.9E-02
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia 		98 9 6 3.3E-02 2 6.9E-02
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 1 9.1E-03 2 6.9E-02