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: C0040962
Disease: Tricuspid Valve Prolapse
Tricuspid Valve Prolapse 		13 4 5 1.3E-02 2 0.20
CUI: C4025752
Disease: Abnormal cardiac ventricle morphology
Abnormal cardiac ventricle morphology 		2 1 2 5.3E-03 1 0.12
CUI: C1836996
Disease: Disproportionate tall stature
Disproportionate tall stature 		30 17 7 1.8E-02 2 8.7E-02
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		82 19 13 2.9E-02 2 8.0E-02
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		102 25 26 5.7E-02 2 6.5E-02
CUI: C4551955
Disease: Loeys-Dietz Syndrome, Type 1a
Loeys-Dietz Syndrome, Type 1a 		5 10 5 1.3E-02 1 5.9E-02
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome 		111 29 24 5.2E-02 2 5.7E-02
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin 		50 11 7 1.7E-02 1 5.6E-02
CUI: C1860493
Disease: Abnormality of the sternum
Abnormality of the sternum 		46 11 15 3.7E-02 1 5.6E-02
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
Abnormality of cardiovascular system morphology 		198 13 16 2.9E-02 1 5.0E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 38 34 5.4E-02 2 4.5E-02
CUI: C1298820
Disease: Aneurysm of aortic root
Aneurysm of aortic root 		39 15 19 4.8E-02 1 4.5E-02
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities 		106 16 18 3.9E-02 1 4.3E-02
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine 		155 17 12 2.3E-02 1 4.2E-02
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 46 4 9.9E-03 2 3.8E-02
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		136 55 25 5.1E-02 2 3.3E-02
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		138 26 15 3.0E-02 1 3.0E-02
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		497 70 26 3.1E-02 2 2.6E-02
CUI: C0042571
Disease: Vertigo
Vertigo 		173 35 33 6.4E-02 1 2.4E-02
CUI: C2697932
Disease: Loeys-Dietz Syndrome
Loeys-Dietz Syndrome 		20 35 13 3.4E-02 1 2.4E-02
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 36 20 3.2E-02 1 2.3E-02
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		69 36 13 3.0E-02 1 2.3E-02
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 53 43 4.7E-02 1 1.7E-02
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 67 5.8E-02 1 7.0E-03
CUI: C0027092
Disease: Myopia
Myopia 		490 167 41 5.0E-02 1 5.7E-03