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: C0232475
Disease: Decreased peristalsis
Decreased peristalsis 		6 0 3 0.38 0 0
CUI: C1855311
Disease: Megacystis
Megacystis 		8 0 3 0.30 0 0
CUI: C1608393
Disease: Megacystis microcolon intestinal hypoperistalsis syndrome
Megacystis microcolon intestinal hypoperistalsis syndrome 		9 0 3 0.27 0 0
CUI: C0042781
Disease: Visceral Myopathy
Visceral Myopathy 		10 19 3 0.25 2 9.5E-02
CUI: C0266200
Disease: Microcolon
Microcolon 		11 2 3 0.23 2 0.50
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 0.20 0 0
CUI: C0265914
Disease: Anomalous pulmonary vein
Anomalous pulmonary vein 		1 0 1 0.20 0 0
CUI: C0266336
Disease: Congenital absence of bladder
Congenital absence of bladder 		1 0 1 0.20 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 0.20 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 0.20 0 0
CUI: C0685828
Disease: Congenital dilatation of bladder
Congenital dilatation of bladder 		1 0 1 0.20 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 0.20 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 0.20 0 0
CUI: C1835084
Disease: Megaduodenum and-or Megacystis
Megaduodenum and-or Megacystis 		1 0 1 0.20 0 0
CUI: C1864996
Disease: Visceral Neuropathy, Familial, Autosomal Dominant
Visceral Neuropathy, Familial, Autosomal Dominant 		1 0 1 0.20 0 0
CUI: C2675862
Disease: Pyloric Stenosis, Infantile Hypertrophic, 5
Pyloric Stenosis, Infantile Hypertrophic, 5 		1 0 1 0.20 0 0
CUI: C3658353
Disease: Nodding Syndrome
Nodding Syndrome 		1 0 1 0.20 0 0
CUI: C0149632
Disease: Abnormality of the bladder
Abnormality of the bladder 		9 2 2 0.17 2 0.50
CUI: C0158638
Disease: Congenital anomaly of cerebrovascular system
Congenital anomaly of cerebrovascular system 		2 0 1 0.17 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 0.17 0 0
CUI: C0392775
Disease: Cystic medial necrosis of aorta
Cystic medial necrosis of aorta 		2 0 1 0.17 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 0.17 0 0
CUI: C1846837
Disease: Aortic Aneurysm, Familial Thoracic 2
Aortic Aneurysm, Familial Thoracic 2 		2 0 1 0.17 0 0
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO 		2 0 1 0.17 0 0
CUI: C3151077
Disease: AORTIC ANEURYSM, FAMILIAL THORACIC 7
AORTIC ANEURYSM, FAMILIAL THORACIC 7 		2 0 1 0.17 0 0