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: C0001122
Disease: Acidosis
Acidosis 		28 0 1 3.1E-02 0 0
CUI: C0002871
Disease: Anemia
Anemia 		847 0 1 1.2E-03 0 0
CUI: C0003962
Disease: Ascites
Ascites 		198 0 1 5.0E-03 0 0
CUI: C0004044
Disease: Asphyxia
Asphyxia 		3 0 1 0.14 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.1E-03 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		106 0 1 9.1E-03 0 0
CUI: C0005859
Disease: Bloom Syndrome
Bloom Syndrome 		155 0 1 6.3E-03 0 0
CUI: C0005941
Disease: Bone Diseases, Developmental
Bone Diseases, Developmental 		82 0 1 1.2E-02 0 0
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		8621 0 1 1.2E-04 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 0 1 2.2E-03 0 0
CUI: C0008311
Disease: Cholangitis
Cholangitis 		80 0 1 1.2E-02 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		611 0 1 1.6E-03 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers 		88 0 1 1.1E-02 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		129 0 1 7.5E-03 0 0
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		488 0 1 2.0E-03 0 0
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		70 0 1 1.4E-02 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 2.6E-02 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		510 0 1 1.9E-03 0 0
CUI: C0013903
Disease: Ellis-Van Creveld Syndrome
Ellis-Van Creveld Syndrome 		11 0 1 6.7E-02 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 1 1.0E-02 0 0
CUI: C0015230
Disease: Exanthema
Exanthema 		251 0 1 3.9E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		1037 0 1 9.6E-04 0 0
CUI: C0016052
Disease: Fibromuscular Dysplasia
Fibromuscular Dysplasia 		47 0 1 2.0E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.3E-02 0 0