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: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 9.7E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 3.6E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		139 0 1 7.2E-03 0 0
CUI: C0003962
Disease: Ascites
Ascites 		198 0 1 5.1E-03 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		384 0 1 2.6E-03 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		106 0 1 9.4E-03 0 0
CUI: C0008311
Disease: Cholangitis
Cholangitis 		80 0 1 1.3E-02 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis 		420 0 1 2.4E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		255 0 1 3.9E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		611 0 1 1.6E-03 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		129 0 1 7.8E-03 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		63 0 1 1.6E-02 0 0
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		488 0 1 2.0E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		725 0 1 1.4E-03 0 0
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		70 0 1 1.4E-02 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 1 7.3E-03 0 0
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		522 0 1 1.9E-03 0 0
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		34 0 1 2.9E-02 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		510 0 1 2.0E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1261 0 1 7.9E-04 0 0
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 1 1.4E-02 0 0
CUI: C0013903
Disease: Ellis-Van Creveld Syndrome
Ellis-Van Creveld Syndrome 		11 0 1 9.1E-02 0 0
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		59 0 1 1.7E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0