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: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 2 2.7E-02 0 0
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome 		77 0 2 2.6E-02 0 0
CUI: C0027643
Disease: Neoplasm Recurrence, Local
Neoplasm Recurrence, Local 		39 0 1 2.5E-02 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 1 2.5E-02 0 0
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		41 0 1 2.4E-02 0 0
CUI: C0277828
Disease: Late fontanel closure
Late fontanel closure 		41 0 1 2.4E-02 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 1 2.2E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		102 0 2 2.0E-02 0 0
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin 		50 0 1 2.0E-02 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 1.9E-02 0 0
CUI: C0423113
Disease: Telecanthus
Telecanthus 		134 0 2 1.5E-02 0 0
CUI: C0032326
Disease: Pneumothorax
Pneumothorax 		69 0 1 1.4E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0
CUI: C1301937
Disease: Talipes
Talipes 		74 0 1 1.3E-02 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 2 1.3E-02 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		77 0 1 1.3E-02 0 0
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		77 0 1 1.3E-02 0 0
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		82 0 1 1.2E-02 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 2 1.2E-02 0 0
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		86 0 1 1.1E-02 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 2 1.1E-02 0 0
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency 		94 0 1 1.1E-02 0 0
CUI: C1853193
Disease: Recurrent skin infections
Recurrent skin infections 		95 0 1 1.0E-02 0 0
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		109 0 1 9.1E-03 0 0
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome 		111 0 1 8.9E-03 0 0