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: C2936381
Disease: Neointima Formation
Neointima Formation 		6 0 6 0.15 0 0
CUI: C3840252
Disease: Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma
Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma 		12 0 5 0.11 0 0
CUI: C0741160
Disease: Aortic Aneurysm, Ruptured
Aortic Aneurysm, Ruptured 		13 0 5 0.10 0 0
CUI: C0003496
Disease: Aortic Rupture
Aortic Rupture 		22 0 5 8.8E-02 0 0
CUI: C0012359
Disease: Pathological Dilatation
Pathological Dilatation 		11 0 4 8.5E-02 0 0
CUI: C0403592
Disease: Chronic rejection of renal transplant
Chronic rejection of renal transplant 		64 0 8 8.3E-02 0 0
CUI: C4020848
Disease: Aneurysmal disease
Aneurysmal disease 		14 0 4 8.0E-02 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 6 7.6E-02 0 0
CUI: C0600518
Disease: Choroidal Neovascularization
Choroidal Neovascularization 		31 0 5 7.6E-02 0 0
CUI: C3150773
Disease: CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME
CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME 		17 0 4 7.5E-02 0 0
CUI: C0087086
Disease: Thrombus
Thrombus 		46 0 6 7.5E-02 0 0
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma 		76 0 8 7.4E-02 0 0
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		34 0 5 7.2E-02 0 0
CUI: C0020542
Disease: Pulmonary Hypertension
Pulmonary Hypertension 		156 0 13 7.1E-02 0 0
CUI: C0020544
Disease: Renal hypertension
Renal hypertension 		36 0 5 7.0E-02 0 0
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy 		115 0 10 6.9E-02 0 0
CUI: C0334096
Disease: Intimal proliferation
Intimal proliferation 		7 0 3 6.8E-02 0 0
CUI: C0729233
Disease: Dissecting aneurysm of the thoracic aorta
Dissecting aneurysm of the thoracic aorta 		57 0 6 6.6E-02 0 0
CUI: C0030848
Disease: Peyronie Disease
Peyronie Disease 		41 0 5 6.6E-02 0 0
CUI: C4721438
Disease: Mitral valve dysplasia
Mitral valve dysplasia 		9 0 3 6.5E-02 0 0
CUI: C4721507
Disease: Alveolitis, Fibrosing
Alveolitis, Fibrosing 		91 0 8 6.5E-02 0 0
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency 		10 0 3 6.4E-02 0 0
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy 		10 0 3 6.4E-02 0 0
CUI: C0041582
Disease: Ulcer
Ulcer 		11 0 3 6.2E-02 0 0
CUI: C0162375
Disease: Granuloma, Giant Cell Reparative
Granuloma, Giant Cell Reparative 		11 0 3 6.2E-02 0 0