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: C4025596
Disease: Abnormality of connective tissue
Abnormality of connective tissue 		4 0 2 0.40 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 0.33 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 0.33 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 0.33 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 0.33 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 0.33 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 0.33 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 0.33 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 0.33 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 0.33 0 0
CUI: C1864738
Disease: Corneal Dystrophy, Congenital Stromal
Corneal Dystrophy, Congenital Stromal 		1 0 1 0.33 0 0
CUI: C2748355
Disease: Descending thoracic aortic dissection
Descending thoracic aortic dissection 		1 0 1 0.33 0 0
CUI: C2931588
Disease: GEMSS syndrome
GEMSS syndrome 		1 0 1 0.33 0 0
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
GELEOPHYSIC DYSPLASIA 2 		1 0 1 0.33 0 0
CUI: C3541518
Disease: ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT 		1 0 1 0.33 0 0
CUI: C3805726
Disease: Medial rotation of the medial malleolus
Medial rotation of the medial malleolus 		1 0 1 0.33 0 0
CUI: C3810451
Disease: Increased corneal thickness
Increased corneal thickness 		1 0 1 0.33 0 0
CUI: C4016052
Disease: MARFAN SYNDROME, SEVERE CLASSIC
MARFAN SYNDROME, SEVERE CLASSIC 		1 0 1 0.33 0 0
CUI: C4016053
Disease: MARFAN SYNDROME, MILD VARIABLE
MARFAN SYNDROME, MILD VARIABLE 		1 0 1 0.33 0 0
CUI: C4016055
Disease: MARFAN SYNDROME, ATYPICAL
MARFAN SYNDROME, ATYPICAL 		1 0 1 0.33 0 0
CUI: C4016056
Disease: MARFAN SYNDROME, MILD
MARFAN SYNDROME, MILD 		1 0 1 0.33 0 0
CUI: C4016059
Disease: MARFAN SYNDROME, AUTOSOMAL RECESSIVE
MARFAN SYNDROME, AUTOSOMAL RECESSIVE 		1 0 1 0.33 0 0
CUI: C4023359
Disease: Abnormal maternal serum screening
Abnormal maternal serum screening 		1 0 1 0.33 0 0
CUI: C4277521
Disease: Cerebrospinal Fluid Hypovolemia
Cerebrospinal Fluid Hypovolemia 		1 0 1 0.33 0 0
CUI: C4310796
Disease: MARFAN LIPODYSTROPHY SYNDROME
MARFAN LIPODYSTROPHY SYNDROME 		1 0 1 0.33 0 0