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: C4021738
Disease: Abnormality of the pubic bone
Abnormality of the pubic bone
4 0 2 0.22 0 0
CUI: C1857002
Disease: Capitate-hamate fusion
Capitate-hamate fusion
8 0 2 0.15 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst
1 2 1 0.14 2 0.67
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors
1 2 1 0.14 2 0.67
CUI: C0333662
Disease: Hemiatrophy
Hemiatrophy
1 0 1 0.14 0 0
CUI: C0543612
Disease: Cervical syndrome
Cervical syndrome
1 0 1 0.14 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder
1 0 1 0.14 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery
1 0 1 0.14 0 0
CUI: C1840013
Disease: Elevated 8-dehydrocholesterol
Elevated 8-dehydrocholesterol
1 0 1 0.14 0 0
CUI: C1840014
Disease: Elevated 8(9)-cholestenol
Elevated 8(9)-cholestenol
1 0 1 0.14 0 0
Increased density of long bone diaphyses
1 0 1 0.14 0 0
CUI: C1844519
Disease: Partial fusion of carpals
Partial fusion of carpals
1 0 1 0.14 0 0
CUI: C1844520
Disease: Partial fusion of tarsals
Partial fusion of tarsals
1 0 1 0.14 0 0
CUI: C1844702
Disease: Vertical clivus
Vertical clivus
1 0 1 0.14 0 0
CUI: C1844712
Disease: Nonossified fifth metatarsal
Nonossified fifth metatarsal
1 0 1 0.14 0 0
Stippled calcification in carpal bones
1 0 1 0.14 0 0
CUI: C1844848
Disease: Tarsal stippling
Tarsal stippling
1 0 1 0.14 0 0
Heterotopia, Periventricular, Ehlers-Danlos Variant
1 0 1 0.14 0 0
Terminal Osseous Dysplasia and Pigmentary Defects
1 0 1 0.14 0 0
CUI: C1862136
Disease: Abnormality of the tarsal bones
Abnormality of the tarsal bones
1 0 1 0.14 0 0
CUI: C1866737
Disease: Lateral femoral bowing
Lateral femoral bowing
1 0 1 0.14 0 0
CUI: C2239253
Disease: Sinus of Valsalva aneurysm
Sinus of Valsalva aneurysm
1 0 1 0.14 0 0
2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase activity
1 0 1 0.14 0 0
Congenital idiopathic intestinal pseudoobstruction
1 0 1 0.14 0 0
CUI: C2748918
Disease: Otopalatodigital Spectrum Disorder
Otopalatodigital Spectrum Disorder
1 0 1 0.14 0 0