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: C0003708
Disease: Arachnoiditis
Arachnoiditis 		1 0 1 7.5E-03 0 0
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis 		1 0 1 7.5E-03 0 0
CUI: C0006897
Disease: Capillariasis
Capillariasis 		1 0 1 7.5E-03 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis 		1 0 1 7.5E-03 0 0
CUI: C0022504
Disease: Kaposi Varicelliform Eruption
Kaposi Varicelliform Eruption 		1 0 1 7.5E-03 0 0
CUI: C0029163
Disease: Oral Hemorrhage
Oral Hemorrhage 		1 0 1 7.5E-03 0 0
CUI: C0030975
Disease: Perceptual Disorders
Perceptual Disorders 		1 0 1 7.5E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 7.5E-03 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness 		1 0 1 7.5E-03 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection 		1 0 1 7.5E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 7.5E-03 0 0
CUI: C0152255
Disease: Pinguecula
Pinguecula 		1 0 1 7.5E-03 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 7.5E-03 0 0
CUI: C0231912
Disease: Nocturnal cough
Nocturnal cough 		1 0 1 7.5E-03 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 7.5E-03 0 0
CUI: C0235242
Disease: Syncope, Effort
Syncope, Effort 		1 0 1 7.5E-03 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 7.5E-03 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 7.5E-03 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 7.5E-03 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 7.5E-03 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 7.5E-03 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 7.5E-03 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 7.5E-03 0 0
CUI: C0271902
Disease: Microcytic normochromic anemia
Microcytic normochromic anemia 		1 0 1 7.5E-03 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 7.5E-03 0 0