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: C0002884
Disease: Hypochromic anemia
Hypochromic anemia 		16 0 1 5.3E-03 0 0
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic 		51 0 1 4.5E-03 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		16 0 1 5.3E-03 0 0
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		22 0 1 5.1E-03 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		1 0 1 5.7E-03 0 0
CUI: C0002940
Disease: Aneurysm
Aneurysm 		22 0 1 5.1E-03 0 0
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 1 5.4E-03 0 0
CUI: C0002985
Disease: Angiokeratoma
Angiokeratoma 		4 0 1 5.6E-03 0 0
CUI: C0002989
Disease: Epithelioid hemangioma of skin
Epithelioid hemangioma of skin 		5 0 1 5.6E-03 0 0
CUI: C0003089
Disease: Ankylosing spondylitis and other inflammatory spondylopathies
Ankylosing spondylitis and other inflammatory spondylopathies 		3 0 1 5.7E-03 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos 		89 0 1 3.8E-03 0 0
CUI: C0003477
Disease: Separation Anxiety Disorder
Separation Anxiety Disorder 		13 0 1 5.4E-03 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		23 0 1 5.1E-03 0 0
CUI: C0003510
Disease: Aortitis Syndrome
Aortitis Syndrome 		2 0 1 5.7E-03 0 0
CUI: C0003621
Disease: Appetite Disorders
Appetite Disorders 		2 0 1 5.7E-03 0 0
CUI: C0003810
Disease: Sertoli-Leydig cell tumor of ovary
Sertoli-Leydig cell tumor of ovary 		5 0 1 5.6E-03 0 0
CUI: C0003834
Disease: Arterial insufficiency
Arterial insufficiency 		2 0 1 5.7E-03 0 0
CUI: C0003875
Disease: Arthritis, Viral
Arthritis, Viral 		3 0 1 5.7E-03 0 0
CUI: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy 		7 0 1 5.6E-03 0 0
CUI: C0003969
Disease: Ascorbic Acid Deficiency
Ascorbic Acid Deficiency 		10 0 1 5.5E-03 0 0
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		23 0 1 5.1E-03 0 0
CUI: C0004310
Disease: Auditory Perceptual Disorders
Auditory Perceptual Disorders 		5 0 1 5.6E-03 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 1 5.2E-03 0 0
CUI: C0004998
Disease: Benign neoplasm of skin
Benign neoplasm of skin 		6 0 1 5.6E-03 0 0
CUI: C0005683
Disease: Urinary Bladder Calculi (disorder)
Urinary Bladder Calculi (disorder) 		10 0 1 5.5E-03 0 0