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: C0240880
Disease: Rectoperineal fistula
Rectoperineal fistula 		2 0 2 0.25 0 0
CUI: C1862698
Disease: Aplasia/Hypoplasia of the 3rd toe
Aplasia/Hypoplasia of the 3rd toe 		2 0 2 0.25 0 0
CUI: C4024162
Disease: Abnormality of the tragus
Abnormality of the tragus 		3 0 2 0.22 0 0
CUI: C0265246
Disease: Townes syndrome
Townes syndrome 		4 0 2 0.20 0 0
CUI: C0426440
Disease: Large nostrils
Large nostrils 		4 2 2 0.20 2 1.00
CUI: C4021029
Disease: Conspicuously happy disposition
Conspicuously happy disposition 		4 0 2 0.20 0 0
CUI: C4021343
Disease: Broad hallux phalanx
Broad hallux phalanx 		17 0 4 0.19 0 0
CUI: C0266345
Disease: Congenital urethral valve
Congenital urethral valve 		5 0 2 0.18 0 0
CUI: C1850327
Disease: Bifid uterus
Bifid uterus 		6 0 2 0.17 0 0
CUI: C4021637
Disease: Abnormality of the nares
Abnormality of the nares 		8 2 2 0.14 2 1.00
CUI: C0266501
Disease: Spina bifida of cervical region
Spina bifida of cervical region 		1 0 1 0.12 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 0.12 0 0
CUI: C0341790
Disease: Neoplasm of scrotum
Neoplasm of scrotum 		1 0 1 0.12 0 0
CUI: C1333859
Disease: Grade 2 Colon Adenocarcinoma
Grade 2 Colon Adenocarcinoma 		1 0 1 0.12 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 0.12 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 10 1 0.12 1 9.1E-02
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C1844516
Disease: Increased density of long bone diaphyses
Increased density of long bone diaphyses 		1 0 1 0.12 0 0
CUI: C1844519
Disease: Partial fusion of carpals
Partial fusion of carpals 		1 0 1 0.12 0 0
CUI: C1844520
Disease: Partial fusion of tarsals
Partial fusion of tarsals 		1 0 1 0.12 0 0
CUI: C1844702
Disease: Vertical clivus
Vertical clivus 		1 0 1 0.12 0 0
CUI: C1844712
Disease: Nonossified fifth metatarsal
Nonossified fifth metatarsal 		1 0 1 0.12 0 0
CUI: C1845235
Disease: Heterotopia, Periventricular, Ehlers-Danlos Variant
Heterotopia, Periventricular, Ehlers-Danlos Variant 		1 0 1 0.12 0 0
CUI: C1846129
Disease: Terminal Osseous Dysplasia and Pigmentary Defects
Terminal Osseous Dysplasia and Pigmentary Defects 		1 0 1 0.12 0 0
CUI: C1862136
Disease: Abnormality of the tarsal bones
Abnormality of the tarsal bones 		1 0 1 0.12 0 0