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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 1.7E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.7E-03
CUI: C0262565
Disease: Anteroseptal Myocardial Infarction
Anteroseptal Myocardial Infarction 		0 1 0 0 1 1.7E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 1.7E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.7E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.7E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 3.4E-03
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0 51 0 0 3 4.7E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 1.7E-03
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0 51 0 0 3 4.7E-03
CUI: C1832465
Disease: Atrophia Maculosa Varioliformis Cutis, Familial
Atrophia Maculosa Varioliformis Cutis, Familial 		0 1 0 0 1 1.7E-03
CUI: C1852324
Disease: ALDOSTERONE TO RENIN RATIO, INCREASED
ALDOSTERONE TO RENIN RATIO, INCREASED 		0 1 0 0 1 1.7E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 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: C4016730
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO 		0 1 0 0 1 1.7E-03
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 5.9E-04 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 5.9E-04 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 5.9E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 5.9E-04 0 0
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 5.9E-04 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 5.9E-04 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 1 5.9E-04 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 1 5.9E-04 0 0