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: C0000821
Disease: Threatened abortion
Threatened abortion 		1 0 1 7.1E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 7.1E-03 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 0 1 7.1E-03 0 0
CUI: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 7.1E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 1 1 7.1E-03 1 7.1E-02
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 7.1E-03 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 0 1 7.1E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 7.1E-03 0 0
CUI: C0221360
Disease: Congenital absence of diaphragm
Congenital absence of diaphragm 		1 0 1 7.1E-03 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 0 1 7.1E-03 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis 		1 0 1 7.1E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 7.1E-03 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 7.1E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 7.1E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 7.1E-03 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 7.1E-03 0 0
CUI: C0266177
Disease: Megaduodenum
Megaduodenum 		1 0 1 7.1E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 7.1E-03 0 0
CUI: C0266429
Disease: Monorchism
Monorchism 		1 0 1 7.1E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 7.1E-03 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 7.1E-03 0 0
CUI: C0348426
Disease: Benign neoplasm of meninges
Benign neoplasm of meninges 		1 0 1 7.1E-03 0 0
CUI: C0406726
Disease: Orofaciodigital syndrome 3
Orofaciodigital syndrome 3 		1 0 1 7.1E-03 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4 		1 0 1 7.1E-03 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 7.1E-03 0 0