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: C1846837
Disease: Aortic Aneurysm, Familial Thoracic 2
Aortic Aneurysm, Familial Thoracic 2 		2 0 2 0.50 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 2 0.50 0 0
CUI: C2673186
Disease: Aortic Aneurysm, Familial Thoracic 6
Aortic Aneurysm, Familial Thoracic 6 		3 16 2 0.40 1 6.2E-02
CUI: C3279690
Disease: MOYAMOYA DISEASE 5
MOYAMOYA DISEASE 5 		3 3 2 0.40 1 0.33
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 0.25 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 0.25 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 0.25 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 0.25 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 0.25 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 0.25 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 0.25 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 0.25 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 0.25 0 0
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 0.20 0 0
CUI: C0158638
Disease: Congenital anomaly of cerebrovascular system
Congenital anomaly of cerebrovascular system 		2 0 1 0.20 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 0.20 0 0
CUI: C0392775
Disease: Cystic medial necrosis of aorta
Cystic medial necrosis of aorta 		2 0 1 0.20 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 0.20 0 0
CUI: C1527298
Disease: Dysentery, Bacillary
Dysentery, Bacillary 		2 0 1 0.20 0 0
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 1 0.20 0 0
CUI: C1844696
Disease: OTOPALATODIGITAL SYNDROME, TYPE II
OTOPALATODIGITAL SYNDROME, TYPE II 		2 0 1 0.20 0 0
CUI: C1846339
Disease: Externally rotated hips
Externally rotated hips 		2 0 1 0.20 0 0
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO 		2 0 1 0.20 0 0
CUI: C3711377
Disease: Intranuclear Rod Myopathy
Intranuclear Rod Myopathy 		2 0 1 0.20 0 0
CUI: C3711389
Disease: Actin-Accumulation Myopathy
Actin-Accumulation Myopathy 		2 0 1 0.20 0 0