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: C0432363
Disease: Shagreen patch
Shagreen patch 		8 0 4 0.19 0 0
CUI: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 3 0.18 0 0
CUI: C4021962
Disease: Genital hernia
Genital hernia 		3 0 3 0.18 0 0
CUI: C0268336
Disease: Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 2 		4 0 3 0.17 0 0
CUI: C4538407
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 		4 0 3 0.17 0 0
CUI: C4552122
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 		5 0 3 0.16 0 0
CUI: C1846545
Disease: Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B 		14 0 4 0.15 0 0
CUI: C0575484
Disease: Long thorax
Long thorax 		9 0 3 0.13 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 3 0.13 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		19 0 4 0.12 0 0
CUI: C1858732
Disease: Malar prominence
Malar prominence 		10 0 3 0.12 0 0
CUI: C4021744
Disease: Abnormality of the wrist
Abnormality of the wrist 		10 0 3 0.12 0 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis 		2 0 2 0.12 0 0
CUI: C2930896
Disease: Congenital thrombotic disease, due to Protein C deficiency
Congenital thrombotic disease, due to Protein C deficiency 		2 0 2 0.12 0 0
CUI: C4225429
Disease: Ehlers-Danlos syndrome classic type
Ehlers-Danlos syndrome classic type 		2 0 2 0.12 0 0
CUI: C4293700
Disease: Subcutaneous spheroids
Subcutaneous spheroids 		2 0 2 0.12 0 0
CUI: C0042909
Disease: Vitreous Hemorrhage
Vitreous Hemorrhage 		12 0 3 0.12 0 0
CUI: C0040046
Disease: Thrombophlebitis
Thrombophlebitis 		3 0 2 0.11 0 0
CUI: C0040962
Disease: Tricuspid Valve Prolapse
Tricuspid Valve Prolapse 		13 0 3 0.11 0 0
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		3 0 2 0.11 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 3 0.11 0 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		3 0 2 0.11 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 3 0.11 0 0
CUI: C0039516
Disease: Tennis Elbow
Tennis Elbow 		4 0 2 0.11 0 0
CUI: C0241657
Disease: Abnormality of the vasculature
Abnormality of the vasculature 		4 0 2 0.11 0 0