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 9.6E-04
Angiotensin converting enzyme measurement
0 1 0 0 1 9.6E-04
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica
1 0 1 2.0E-03 0 0
CUI: C0149756
Disease: Fasciitis, Plantar
Fasciitis, Plantar
1 0 1 2.0E-03 0 0
Chronic obstructive asthma (with obstructive pulmonary disease)
1 0 1 2.0E-03 0 0
CUI: C0158360
Disease: Fibromatosis, Plantar
Fibromatosis, Plantar
1 0 1 2.0E-03 0 0
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart
1 0 1 2.0E-03 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement
1 0 1 2.0E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
1 0 1 2.0E-03 0 0
CUI: C0442840
Disease: Cardiac embolism
Cardiac embolism
1 0 1 2.0E-03 0 0
Congenital malformation of cardiac chambers and connections, unspecified
1 0 1 2.0E-03 0 0
Reaction to severe stress, and adjustment disorders
1 0 1 2.0E-03 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement
1 0 1 2.0E-03 0 0
CUI: C0523801
Disease: Ornithine measurement
Ornithine measurement
1 0 1 2.0E-03 0 0
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
1 0 1 2.0E-03 0 0
CUI: C1531500
Disease: Alpha carotene level
Alpha carotene level
1 0 1 2.0E-03 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
1 0 1 2.0E-03 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
1 0 1 2.0E-03 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2
1 0 1 2.0E-03 0 0
Modic type vertebral endplate changes
1 0 1 2.0E-03 0 0
HIV-associated neurocognitive disorder
1 0 1 2.0E-03 0 0
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia
2 0 1 2.0E-03 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
2 0 1 2.0E-03 0 0
CUI: C0149516
Disease: Chronic sinusitis
Chronic sinusitis
2 0 1 2.0E-03 0 0
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
2 0 1 2.0E-03 0 0