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: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 3 0.30 0 0
CUI: C4021962
Disease: Genital hernia
Genital hernia 		3 0 3 0.30 0 0
CUI: C4538407
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 		4 0 3 0.27 0 0
CUI: C4552122
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 		5 0 3 0.25 0 0
CUI: C0432363
Disease: Shagreen patch
Shagreen patch 		8 0 3 0.20 0 0
CUI: C4225429
Disease: Ehlers-Danlos syndrome classic type
Ehlers-Danlos syndrome classic type 		2 0 2 0.20 0 0
CUI: C4293700
Disease: Subcutaneous spheroids
Subcutaneous spheroids 		2 0 2 0.20 0 0
CUI: C0575484
Disease: Long thorax
Long thorax 		9 0 3 0.19 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 3 0.19 0 0
CUI: C1839736
Disease: WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME
WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME 		3 0 2 0.18 0 0
CUI: C0039516
Disease: Tennis Elbow
Tennis Elbow 		4 0 2 0.17 0 0
CUI: C0268335
Disease: Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 1 		4 0 2 0.17 0 0
CUI: C0268336
Disease: Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 2 		4 0 2 0.17 0 0
CUI: C1844597
Disease: Molluscoid pseudotumors
Molluscoid pseudotumors 		5 0 2 0.15 0 0
CUI: C1851828
Disease: Cigarette-paper scars
Cigarette-paper scars 		5 0 2 0.15 0 0
CUI: C1860105
Disease: Severe short-limb dwarfism
Severe short-limb dwarfism 		5 0 2 0.15 0 0
CUI: C0040962
Disease: Tricuspid Valve Prolapse
Tricuspid Valve Prolapse 		13 0 3 0.15 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 3 0.15 0 0
CUI: C0019555
Disease: Hip Dislocation, Congenital
Hip Dislocation, Congenital 		6 0 2 0.14 0 0
CUI: C1846545
Disease: Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B 		14 0 3 0.14 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 3 0.14 0 0
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		17 0 3 0.12 0 0
CUI: C0410787
Disease: Hereditary Connective Tissue Disorder
Hereditary Connective Tissue Disorder 		9 0 2 0.12 0 0
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		11 0 2 0.11 0 0
CUI: C0002940
Disease: Aneurysm
Aneurysm 		22 0 3 0.10 0 0