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: C4021884
Disease: Bilateral choanal atresia/stenosis
Bilateral choanal atresia/stenosis 		3 0 2 0.50 0 0
CUI: C1832390
Disease: Van Maldergem Wetzburger Verloes syndrome
Van Maldergem Wetzburger Verloes syndrome 		4 0 2 0.40 0 0
CUI: C1849173
Disease: Periventricular gray matter heterotopia
Periventricular gray matter heterotopia 		4 0 2 0.40 0 0
CUI: C1843003
Disease: MITRAL VALVE PROLAPSE, MYXOMATOUS 2
MITRAL VALVE PROLAPSE, MYXOMATOUS 2 		1 0 1 0.33 0 0
CUI: C3809875
Disease: VAN MALDERGEM SYNDROME 2
VAN MALDERGEM SYNDROME 2 		1 0 1 0.33 0 0
CUI: C4014939
Disease: HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2 		1 0 1 0.33 0 0
CUI: C4551950
Disease: VAN MALDERGEM SYNDROME 1
VAN MALDERGEM SYNDROME 1 		1 0 1 0.33 0 0
CUI: C1856765
Disease: Irregular dentition
Irregular dentition 		6 0 2 0.29 0 0
CUI: C3277117
Disease: Caudal appendage
Caudal appendage 		6 0 2 0.29 0 0
CUI: C1856140
Disease: Pericardial lymphangiectasia
Pericardial lymphangiectasia 		2 0 1 0.25 0 0
CUI: C1848514
Disease: Short fourth metatarsal
Short fourth metatarsal 		8 0 2 0.22 0 0
CUI: C4012050
Disease: HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1 		3 0 1 0.20 0 0
CUI: C0410935
Disease: Wide cranial sutures
Wide cranial sutures 		10 0 2 0.18 0 0
CUI: C1855480
Disease: Pulmonary lymphangiectasia
Pulmonary lymphangiectasia 		4 0 1 0.17 0 0
CUI: C1840309
Disease: Short 4th metacarpal
Short 4th metacarpal 		14 0 2 0.13 0 0
CUI: C0024215
Disease: Lymphangiectasis, Intestinal
Lymphangiectasis, Intestinal 		6 0 1 0.12 0 0
CUI: C0266304
Disease: Double kidney (disorder)
Double kidney (disorder) 		6 0 1 0.12 0 0
CUI: C0340834
Disease: Hennekam lymphangiectasia-lymphedema syndrome
Hennekam lymphangiectasia-lymphedema syndrome 		6 0 1 0.12 0 0
CUI: C1835580
Disease: Mild postnatal growth retardation
Mild postnatal growth retardation 		6 0 1 0.12 0 0
CUI: C4551969
Disease: Bilateral Periventricular Nodular Heterotopia
Bilateral Periventricular Nodular Heterotopia 		6 0 1 0.12 0 0
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		20 0 2 9.5E-02 0 0
CUI: C0340364
Disease: Familial mitral valve prolapse
Familial mitral valve prolapse 		10 0 1 8.3E-02 0 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development 		24 0 2 8.0E-02 0 0
CUI: C0431369
Disease: Dysgenesis of corpus callosum
Dysgenesis of corpus callosum 		25 0 2 7.7E-02 0 0
CUI: C0426807
Disease: Short clavicle
Short clavicle 		26 0 2 7.4E-02 0 0