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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
0 4 0 0 1 5.2E-04
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia
0 11 0 0 1 5.2E-04
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 5.2E-04
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia
0 1 0 0 1 5.2E-04
Angiotensin converting enzyme measurement
0 1 0 0 1 5.2E-04
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test
0 3 0 0 1 5.2E-04
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 5.2E-04
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 5.2E-04
Deficiency of butyryl-CoA dehydrogenase
0 47 0 0 1 5.1E-04
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 5.2E-04
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 5.2E-04
CUI: C0854135
Disease: Pseudomonas aeruginosa infection
Pseudomonas aeruginosa infection
0 1 0 0 1 5.2E-04
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 5.2E-04
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 5.2E-04
CUI: C1281440
Disease: Familial obesity
Familial obesity
0 3 0 0 1 5.2E-04
CUI: C1623258
Disease: Electrocardiography
Electrocardiography
0 16 0 0 1 5.1E-04
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity
0 3 0 0 1 5.2E-04
CUI: C4285890
Disease: Carotid artery calcification
Carotid artery calcification
0 3 0 0 1 5.2E-04
CUI: C0000821
Disease: Threatened abortion
Threatened abortion
1 0 1 1.2E-03 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis
22 0 1 1.2E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 1.2E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 1.1E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 1.2E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 1.2E-03 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis
5 0 1 1.2E-03 0 0