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: C2931803
Disease: Deletion 11p13
Deletion 11p13 		3 0 3 0.12 0 0
CUI: C1832671
Disease: Dysfunction of lateral corticospinal tracts
Dysfunction of lateral corticospinal tracts 		4 0 3 0.12 0 0
CUI: C1840452
Disease: Hyaloideoretinal degeneration of Wagner
Hyaloideoretinal degeneration of Wagner 		7 0 3 0.11 0 0
CUI: C0269011
Disease: Increased size of penis
Increased size of penis 		12 0 3 9.1E-02 0 0
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		13 0 3 8.8E-02 0 0
CUI: C0278184
Disease: Scanning speech
Scanning speech 		13 0 3 8.8E-02 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 3 8.6E-02 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 2 8.3E-02 0 0
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities 		42 0 5 8.2E-02 0 0
CUI: C1861218
Disease: Hypoplastic ilia
Hypoplastic ilia 		16 0 3 8.1E-02 0 0
CUI: C0265282
Disease: Fibrochondrogenesis
Fibrochondrogenesis 		3 0 2 8.0E-02 0 0
CUI: C1274879
Disease: Port-wine stain with oculocutaneous melanosis
Port-wine stain with oculocutaneous melanosis 		3 0 2 8.0E-02 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 2 8.0E-02 0 0
CUI: C1859882
Disease: Pigmentation of the sclera
Pigmentation of the sclera 		3 0 2 8.0E-02 0 0
CUI: C0263417
Disease: Cutis verticis gyrata
Cutis verticis gyrata 		4 0 2 7.7E-02 0 0
CUI: C0344542
Disease: Aniridia type 1
Aniridia type 1 		4 0 2 7.7E-02 0 0
CUI: C0431401
Disease: Gillespie syndrome
Gillespie syndrome 		4 0 2 7.7E-02 0 0
CUI: C1858084
Disease: STICKLER SYNDROME, TYPE II (disorder)
STICKLER SYNDROME, TYPE II (disorder) 		4 0 2 7.7E-02 0 0
CUI: C1863402
Disease: Broad distal phalanx of the thumb
Broad distal phalanx of the thumb 		4 0 2 7.7E-02 0 0
CUI: C0265985
Disease: Mongolian Spot
Mongolian Spot 		5 3 2 7.4E-02 1 0.14
CUI: C0235986
Disease: Growth hormone excess
Growth hormone excess 		20 0 3 7.3E-02 0 0
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		6 0 2 7.1E-02 0 0
CUI: C0345375
Disease: Congenital hypoplasia of femur
Congenital hypoplasia of femur 		22 0 3 7.0E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 3 6.5E-02 0 0
CUI: C1865186
Disease: Bell-shaped thorax
Bell-shaped thorax 		26 0 3 6.4E-02 0 0