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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.7E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.7E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.7E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 1.7E-03
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 1.7E-03
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0 46 0 0 4 6.3E-03
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement 		0 11 0 0 1 1.7E-03
CUI: C2699063
Disease: Resistin Measurement
Resistin Measurement 		0 6 0 0 1 1.7E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.7E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-03
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism 		0 2 0 0 1 1.7E-03
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 8.4E-04 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 8.5E-04 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		55 0 1 8.5E-04 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 8.5E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 8.5E-04 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 8.5E-04 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 8.6E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 8.6E-04 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 8.6E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 8.6E-04 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 8.6E-04 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 8.6E-04 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 1 8.6E-04 0 0