Source: INFERRED ×
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 8.8E-04
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		0 3 0 0 1 8.8E-04
CUI: C0373601
Disease: Dihydrotestosterone Assay
Dihydrotestosterone Assay 		0 2 0 0 1 8.8E-04
CUI: C0004610
Disease: Bacteremia
Bacteremia 		1 0 1 1.8E-03 0 0
CUI: C0015190
Disease: Euthyroid Sick Syndromes
Euthyroid Sick Syndromes 		1 0 1 1.8E-03 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		1 0 1 1.8E-03 0 0
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		1 0 1 1.8E-03 0 0
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I 		1 0 1 1.8E-03 0 0
CUI: C0029878
Disease: Otitis Externa
Otitis Externa 		1 0 1 1.8E-03 0 0
CUI: C0030286
Disease: Pancreatic Diseases
Pancreatic Diseases 		1 0 1 1.8E-03 0 0
CUI: C0030508
Disease: Parasomnia
Parasomnia 		1 0 1 1.8E-03 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 1.8E-03 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		1 0 1 1.8E-03 0 0
CUI: C0086664
Disease: Myelocele
Myelocele 		1 0 1 1.8E-03 0 0
CUI: C0149756
Disease: Fasciitis, Plantar
Fasciitis, Plantar 		1 0 1 1.8E-03 0 0
CUI: C0152443
Disease: Urethral diverticulum
Urethral diverticulum 		1 0 1 1.8E-03 0 0
CUI: C0155196
Disease: Cicatricial ectropion
Cicatricial ectropion 		1 0 1 1.8E-03 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 1.8E-03 0 0
CUI: C0158360
Disease: Fibromatosis, Plantar
Fibromatosis, Plantar 		1 0 1 1.8E-03 0 0
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart 		1 0 1 1.8E-03 0 0
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria 		1 0 1 1.8E-03 0 0
CUI: C0220754
Disease: Biotinidase Deficiency
Biotinidase Deficiency 		1 0 1 1.8E-03 0 0
CUI: C0221055
Disease: Paramyotonia Congenita (disorder)
Paramyotonia Congenita (disorder) 		1 0 1 1.8E-03 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 1.8E-03 0 0
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis 		1 0 1 1.8E-03 0 0