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: C0302883
Disease: SMITH DISEASE
SMITH DISEASE 		1 0 1 1.00 0 0
CUI: C0345982
Disease: Multiple self-healing epithelioma of Ferguson-Smith
Multiple self-healing epithelioma of Ferguson-Smith 		1 0 1 1.00 0 0
CUI: C3898580
Disease: Loeys-Dietz Syndrome Type 2
Loeys-Dietz Syndrome Type 2 		2 0 1 0.50 0 0
CUI: C4025752
Disease: Abnormal cardiac ventricle morphology
Abnormal cardiac ventricle morphology 		2 0 1 0.50 0 0
CUI: C4749284
Disease: Familial bicuspid aortic valve
Familial bicuspid aortic valve 		3 0 1 0.33 0 0
CUI: C0042143
Disease: Uterine Rupture
Uterine Rupture 		4 0 1 0.25 0 0
CUI: C0155676
Disease: Pulmonary artery aneurysm
Pulmonary artery aneurysm 		4 0 1 0.25 0 0
CUI: C1836651
Disease: Generalized arterial tortuosity
Generalized arterial tortuosity 		4 0 1 0.25 0 0
CUI: C1861559
Disease: CHROMATE RESISTANCE (disorder)
CHROMATE RESISTANCE (disorder) 		4 0 1 0.25 0 0
CUI: C1836635
Disease: Loeys-Dietz Aortic Aneurysm Syndrome
Loeys-Dietz Aortic Aneurysm Syndrome 		5 0 1 0.20 0 0
CUI: C4277533
Disease: Dissection, Blood Vessel
Dissection, Blood Vessel 		5 0 1 0.20 0 0
CUI: C4551955
Disease: Loeys-Dietz Syndrome, Type 1a
Loeys-Dietz Syndrome, Type 1a 		5 10 1 0.20 1 6.7E-02
CUI: C4552122
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 		5 0 1 0.20 0 0
CUI: C4703646
Disease: Eosinophilic infiltration of the esophagus
Eosinophilic infiltration of the esophagus 		5 0 1 0.20 0 0
CUI: C0546476
Disease: Multiple self-healing squamous epithelioma
Multiple self-healing squamous epithelioma 		6 0 1 0.17 0 0
CUI: C0333227
Disease: Microembolus
Microembolus 		7 0 1 0.14 0 0
CUI: C0813148
Disease: Metastatic Endometrial Carcinoma
Metastatic Endometrial Carcinoma 		7 0 1 0.14 0 0
CUI: C2350038
Disease: Molar Incisor Hypomineralization
Molar Incisor Hypomineralization 		7 0 1 0.14 0 0
CUI: C4330043
Disease: Gingival Squamous Cell Carcinoma
Gingival Squamous Cell Carcinoma 		8 0 1 0.12 0 0
CUI: C0008449
Disease: Congenital anomaly of cartilage
Congenital anomaly of cartilage 		9 0 1 0.11 0 0
CUI: C0340364
Disease: Familial mitral valve prolapse
Familial mitral valve prolapse 		10 0 1 1.0E-01 0 0
CUI: C1836646
Disease: Dermal translucency
Dermal translucency 		10 0 1 1.0E-01 0 0
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I 		11 0 1 9.1E-02 0 0
CUI: C0012817
Disease: Diverticulum
Diverticulum 		12 0 1 8.3E-02 0 0
CUI: C0013743
Disease: Eisenmenger Complex
Eisenmenger Complex 		13 0 1 7.7E-02 0 0