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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 6.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 6.8E-03
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 6.8E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 6.8E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 6.7E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 6.8E-03
CUI: C0865791
Disease: Obstructive bronchitis
Obstructive bronchitis
0 1 0 0 1 6.8E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 6.7E-03
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF
0 1 0 0 1 6.8E-03
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF
0 1 0 0 1 6.8E-03
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
0 1 0 0 1 6.8E-03
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 6.8E-03
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 6.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 6.7E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 6.8E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 6.8E-03
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
0 1 0 0 1 6.8E-03
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute
2 0 1 1.1E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 1.1E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 1.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 1.1E-03 0 0
CUI: C0001145
Disease: Acne Keloid
Acne Keloid
1 0 1 1.1E-03 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis
5 0 1 1.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 1.1E-03 0 0
Herpetic Acute Necrotizing Encephalitis
5 0 1 1.1E-03 0 0