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: C0751859
Disease: Lead Poisoning, Nervous System
Lead Poisoning, Nervous System 		2 0 1 0.33 0 0
CUI: C1867132
Disease: Plantar crease between first and second toes
Plantar crease between first and second toes 		2 0 1 0.33 0 0
CUI: C4025806
Disease: High axial triradius
High axial triradius 		2 0 1 0.33 0 0
CUI: C4551859
Disease: RUBINSTEIN-TAYBI SYNDROME 1
RUBINSTEIN-TAYBI SYNDROME 1 		2 39 1 0.33 1 1.4E-02
CUI: C1290508
Disease: Abnormal number of teeth
Abnormal number of teeth 		3 0 1 0.25 0 0
CUI: C4025111
Disease: Radial deviation of thumb terminal phalanx
Radial deviation of thumb terminal phalanx 		3 0 1 0.25 0 0
CUI: C0399357
Disease: Talon cusp
Talon cusp 		5 0 1 0.17 0 0
CUI: C0549397
Disease: Deviated nasal septum
Deviated nasal septum 		5 0 1 0.17 0 0
CUI: C1844508
Disease: Large foramen magnum
Large foramen magnum 		6 0 1 0.14 0 0
CUI: C1850327
Disease: Bifid uterus
Bifid uterus 		6 0 1 0.14 0 0
CUI: C1860164
Disease: Duplication of phalanx of hallux
Duplication of phalanx of hallux 		6 0 1 0.14 0 0
CUI: C4024221
Disease: Papillary cystadenoma of the epididymis
Papillary cystadenoma of the epididymis 		6 0 1 0.14 0 0
CUI: C0425772
Disease: Premature development of the breasts
Premature development of the breasts 		7 0 1 0.12 0 0
CUI: C1857126
Disease: Parietal bossing
Parietal bossing 		7 1 1 0.12 1 3.2E-02
CUI: C1857627
Disease: Chorioretinal dystrophy
Chorioretinal dystrophy 		7 0 1 0.12 0 0
CUI: C0024454
Disease: Maffucci Syndrome
Maffucci Syndrome 		8 0 1 0.11 0 0
CUI: C0221214
Disease: Vascular ring
Vascular ring 		8 0 1 0.11 0 0
CUI: C1185616
Disease: Hair whorls
Hair whorls 		9 0 1 1.0E-01 0 0
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology 		9 0 1 1.0E-01 0 0
CUI: C4021539
Disease: Posterior helix pit
Posterior helix pit 		9 0 1 1.0E-01 0 0
CUI: C0234853
Disease: Facial grimacing
Facial grimacing 		10 0 1 9.1E-02 0 0
CUI: C0027612
Disease: Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 		12 0 1 7.7E-02 0 0
CUI: C1281931
Disease: Obstruction of nasolacrimal duct
Obstruction of nasolacrimal duct 		12 0 1 7.7E-02 0 0
CUI: C1527348
Disease: Brain Hypoxia
Brain Hypoxia 		12 0 1 7.7E-02 0 0
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine 		12 0 1 7.7E-02 0 0