Source: CURATED ×
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: C1858556
Disease: OVERLAP CONNECTIVE TISSUE DISEASE
OVERLAP CONNECTIVE TISSUE DISEASE 		1 26 1 1.00 22 0.79
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 26 1 1.00 22 0.79
CUI: C2931588
Disease: GEMSS syndrome
GEMSS syndrome 		1 0 1 1.00 0 0
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
GELEOPHYSIC DYSPLASIA 2 		1 27 1 1.00 22 0.76
CUI: C4016054
Disease: Neonatal Marfan syndrome
Neonatal Marfan syndrome 		1 0 1 1.00 0 0
CUI: C4310796
Disease: MARFAN LIPODYSTROPHY SYNDROME
MARFAN LIPODYSTROPHY SYNDROME 		1 27 1 1.00 22 0.76
CUI: C0013581
Disease: Ectopia Lentis
Ectopia Lentis 		2 7 1 0.50 1 3.3E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		2 0 1 0.50 0 0
CUI: C1851286
Disease: Ectopia lentis isolated
Ectopia lentis isolated 		2 0 1 0.50 0 0
CUI: C2746069
Disease: Familial ectopia lentis
Familial ectopia lentis 		2 0 1 0.50 0 0
CUI: C0265313
Disease: Weill-Marchesani syndrome
Weill-Marchesani syndrome 		3 0 1 0.33 0 0
CUI: C1869114
Disease: Weill-Marchesani Syndrome, Autosomal Recessive
Weill-Marchesani Syndrome, Autosomal Recessive 		3 0 1 0.33 0 0
CUI: C1869115
Disease: Weill-Marchesani Syndrome, Autosomal Dominant
Weill-Marchesani Syndrome, Autosomal Dominant 		3 23 1 0.33 22 0.88
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		4 0 1 0.25 0 0
CUI: C0003496
Disease: Aortic Rupture
Aortic Rupture 		5 0 1 0.20 0 0
CUI: C0265287
Disease: Acromicric Dysplasia
Acromicric Dysplasia 		5 27 1 0.20 22 0.76
CUI: C0741160
Disease: Aortic Aneurysm, Ruptured
Aortic Aneurysm, Ruptured 		5 0 1 0.20 0 0
CUI: C3489726
Disease: Geleophysic dysplasia
Geleophysic dysplasia 		5 0 1 0.20 0 0
CUI: C0162872
Disease: Aortic Aneurysm, Thoracic
Aortic Aneurysm, Thoracic 		7 0 1 0.14 0 0
CUI: C0340630
Disease: Aortic Aneurysm, Thoracoabdominal
Aortic Aneurysm, Thoracoabdominal 		7 0 1 0.14 0 0
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I 		9 0 1 0.11 0 0
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		11 997 1 9.1E-02 24 2.4E-02
CUI: C1257963
Disease: Endogenous Hyperinsulinism
Endogenous Hyperinsulinism 		26 0 1 3.8E-02 0 0
CUI: C1257964
Disease: Exogenous Hyperinsulinism
Exogenous Hyperinsulinism 		26 0 1 3.8E-02 0 0
CUI: C1257965
Disease: Compensatory Hyperinsulinemia
Compensatory Hyperinsulinemia 		26 0 1 3.8E-02 0 0