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: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 0.14 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 0.14 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 0.14 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 0.14 0 0
CUI: C0268356
Disease: Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta with blue sclerae AND normal teeth 		1 0 1 0.14 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 0.14 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 0.14 0 0
CUI: C0345002
Disease: Quadricuspid aortic valve
Quadricuspid aortic valve 		1 0 1 0.14 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 0.14 0 0
CUI: C0451818
Disease: Dietary zinc deficiency
Dietary zinc deficiency 		1 0 1 0.14 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 0.14 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 0.14 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 0.14 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 0.14 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage 		1 0 1 0.14 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 0.14 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 0.14 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 0.14 0 0
CUI: C1851811
Disease: Hypermobility of distal interphalangeal joints
Hypermobility of distal interphalangeal joints 		1 0 1 0.14 0 0
CUI: C1852924
Disease: OI-EDS Combined Syndrome
OI-EDS Combined Syndrome 		1 0 1 0.14 0 0
CUI: C1853365
Disease: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1 		1 0 1 0.14 0 0
CUI: C1857034
Disease: Ehlers-Danlos syndrome, cardiac valvular form
Ehlers-Danlos syndrome, cardiac valvular form 		1 0 1 0.14 0 0
CUI: C1859069
Disease: Brittle Bone Disorder
Brittle Bone Disorder 		1 0 1 0.14 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 0.14 0 0
CUI: C1866507
Disease: Spondyloepimetaphyseal Dysplasia With Abnormal Dentition
Spondyloepimetaphyseal Dysplasia With Abnormal Dentition 		1 0 1 0.14 0 0