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: C0022361
Disease: Jaw Cysts
Jaw Cysts 		3 0 1 0.20 0 0
CUI: C0264272
Disease: Purulent rhinitis
Purulent rhinitis 		3 0 1 0.20 0 0
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		3 0 1 0.20 0 0
CUI: C0268646
Disease: Isolated cystinuria
Isolated cystinuria 		3 0 1 0.20 0 0
CUI: C0752144
Disease: Brain Thrombosis
Brain Thrombosis 		3 0 1 0.20 0 0
CUI: C0796081
Disease: Myhre syndrome
Myhre syndrome 		3 0 1 0.20 0 0
CUI: C0856904
Disease: Allergy to fish
Allergy to fish 		3 0 1 0.20 0 0
CUI: C0936263
Disease: Cerebral Thrombus
Cerebral Thrombus 		3 0 1 0.20 0 0
CUI: C1848745
Disease: Oliver-McFarlane syndrome
Oliver-McFarlane syndrome 		3 0 1 0.20 0 0
CUI: C1853144
Disease: Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia 		3 0 1 0.20 0 0
CUI: C1859372
Disease: Calcification of Joints and Arteries
Calcification of Joints and Arteries 		3 0 1 0.20 0 0
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy 		3 0 1 0.20 0 0
CUI: C2586031
Disease: Hereditary antithrombin III deficiency
Hereditary antithrombin III deficiency 		3 0 1 0.20 0 0
CUI: C3658294
Disease: Hereditary Antithrombin Deficiency
Hereditary Antithrombin Deficiency 		3 0 1 0.20 0 0
CUI: C3850155
Disease: Congenital Microtia
Congenital Microtia 		3 0 1 0.20 0 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		3 0 1 0.20 0 0
CUI: C0030105
Disease: Ozena (disorder)
Ozena (disorder) 		4 0 1 0.17 0 0
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 1 0.17 0 0
CUI: C0428282
Disease: Serum creatinine low
Serum creatinine low 		4 0 1 0.17 0 0
CUI: C0024904
Disease: Mastoiditis
Mastoiditis 		5 0 1 0.14 0 0
CUI: C0396072
Disease: Laryngeal papillomatosis
Laryngeal papillomatosis 		5 0 1 0.14 0 0
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus 		5 0 1 0.14 0 0
CUI: C1274224
Disease: Inherited epidermolysis bullosa
Inherited epidermolysis bullosa 		5 0 1 0.14 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 1 0.14 0 0
CUI: C1865145
Disease: Congenital disorder of glycosylation type 1B
Congenital disorder of glycosylation type 1B 		5 0 1 0.14 0 0