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 4.2E-03
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 4.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 4.2E-03
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0 77 0 0 1 3.2E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 8.4E-03
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0 77 0 0 1 3.2E-03
CUI: C1969115
Disease: GALLBLADDER DISEASE 4
GALLBLADDER DISEASE 4 		0 1 0 0 1 4.2E-03
CUI: C2609268
Disease: Low phospholipid-associated cholelithiasis
Low phospholipid-associated cholelithiasis 		0 29 0 0 1 3.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 3 1.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.2E-03
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 7.8E-04 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 7.9E-04 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 7.9E-04 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 7.9E-04 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 8.0E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 8.0E-04 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 8.0E-04 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 8.1E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 8.1E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 8.1E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 8.1E-04 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 8.1E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 8.1E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 8.1E-04 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 8.1E-04 0 0