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: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 1.9E-02 0 0
CUI: C1275417
Disease: Non-involuting congenital hemangioma
Non-involuting congenital hemangioma 		1 0 1 1.9E-02 0 0
CUI: C1302778
Disease: Congenital lymphatic malformation
Congenital lymphatic malformation 		1 0 1 1.9E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 1.9E-02 0 0
CUI: C1306574
Disease: Botryoid rhabdomyosarcoma
Botryoid rhabdomyosarcoma 		1 0 1 1.9E-02 0 0
CUI: C1321871
Disease: childhood acute myeloid leukemia/other myeloid malignancies
childhood acute myeloid leukemia/other myeloid malignancies 		1 0 1 1.9E-02 0 0
CUI: C1333081
Disease: Colloid Carcinoma of the Pancreas
Colloid Carcinoma of the Pancreas 		1 0 1 1.9E-02 0 0
CUI: C1333308
Disease: Distal Bile Duct Carcinoma
Distal Bile Duct Carcinoma 		1 0 1 1.9E-02 0 0
CUI: C1334691
Disease: Melanomatosis
Melanomatosis 		1 0 1 1.9E-02 0 0
CUI: C1517445
Disease: Ganglioneuroblastoma, Nodular
Ganglioneuroblastoma, Nodular 		1 0 1 1.9E-02 0 0
CUI: C1704453
Disease: Oncocytic Schneiderian papilloma
Oncocytic Schneiderian papilloma 		1 0 1 1.9E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 0 1 1.9E-02 0 0
CUI: C1837464
Disease: Small eyes
Small eyes 		1 0 1 1.9E-02 0 0
CUI: C1838257
Disease: Serpentine fibula polycystic kidney syndrome
Serpentine fibula polycystic kidney syndrome 		1 0 1 1.9E-02 0 0
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		1 0 1 1.9E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 1.9E-02 0 0
CUI: C1842084
Disease: Posterior rib fusion
Posterior rib fusion 		1 0 1 1.9E-02 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 1.9E-02 0 0
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root 		1 0 1 1.9E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 1.9E-02 0 0
CUI: C1844516
Disease: Increased density of long bone diaphyses
Increased density of long bone diaphyses 		1 0 1 1.9E-02 0 0
CUI: C1844519
Disease: Partial fusion of carpals
Partial fusion of carpals 		1 0 1 1.9E-02 0 0
CUI: C1844520
Disease: Partial fusion of tarsals
Partial fusion of tarsals 		1 0 1 1.9E-02 0 0
CUI: C1844702
Disease: Vertical clivus
Vertical clivus 		1 0 1 1.9E-02 0 0
CUI: C1844712
Disease: Nonossified fifth metatarsal
Nonossified fifth metatarsal 		1 0 1 1.9E-02 0 0