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: C1395674
Disease: Bowel diverticulosis
Bowel diverticulosis 		5 0 4 0.31 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		3 0 3 0.25 0 0
CUI: C2931134
Disease: Cutis laxa, recessive
Cutis laxa, recessive 		3 0 3 0.25 0 0
CUI: C3665335
Disease: Cutis laxa, autosomal recessive
Cutis laxa, autosomal recessive 		17 0 5 0.21 0 0
CUI: C1857710
Disease: Progeroid facial appearance
Progeroid facial appearance 		14 0 4 0.18 0 0
CUI: C0268351
Disease: Cutis Laxa, Autosomal Recessive, Type I
Cutis Laxa, Autosomal Recessive, Type I 		2 0 2 0.17 0 0
CUI: C0432336
Disease: Cutis laxa, recessive, type I
Cutis laxa, recessive, type I 		2 0 2 0.17 0 0
CUI: C2315541
Disease: Diverticulum of renal calyx
Diverticulum of renal calyx 		2 0 2 0.17 0 0
CUI: C1836646
Disease: Dermal translucency
Dermal translucency 		10 0 3 0.16 0 0
CUI: C0156273
Disease: Bladder Diverticulum
Bladder Diverticulum 		18 0 4 0.15 0 0
CUI: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		3 0 2 0.15 0 0
CUI: C0406586
Disease: Wiedemann-Rautenstrauch syndrome
Wiedemann-Rautenstrauch syndrome 		3 0 2 0.15 0 0
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat 		11 0 3 0.15 0 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge 		11 0 3 0.15 0 0
CUI: C0264133
Disease: Acquired flat foot
Acquired flat foot 		4 0 2 0.14 0 0
CUI: C1848771
Disease: Prominent superficial blood vessels
Prominent superficial blood vessels 		4 0 2 0.14 0 0
CUI: C1837767
Disease: Loss of facial adipose tissue
Loss of facial adipose tissue 		6 0 2 0.12 0 0
CUI: C1856542
Disease: Prominent scalp veins
Prominent scalp veins 		6 0 2 0.12 0 0
CUI: C1857657
Disease: Reduced subcutaneous adipose tissue
Reduced subcutaneous adipose tissue 		21 0 3 1.0E-01 0 0
CUI: C0042140
Disease: Uterine Prolapse
Uterine Prolapse 		12 0 2 9.1E-02 0 0
CUI: C0581342
Disease: Redundant skin
Redundant skin 		48 0 5 9.1E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 8.3E-02 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome 		1 0 1 8.3E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 8.3E-02 0 0
CUI: C0795932
Disease: fontaine syndrome
fontaine syndrome 		1 0 1 8.3E-02 0 0