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: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.6E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.6E-02
CUI: C1333046
Disease: Myeloproliferative Neoplasm, Unclassifiable
Myeloproliferative Neoplasm, Unclassifiable 		0 3 0 0 2 3.1E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 3.2E-02
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute 		2 0 1 1.6E-03 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass 		2 0 1 1.6E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.6E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 1.6E-03 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis 		5 0 1 1.6E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 1.6E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.6E-03 0 0
CUI: C0001529
Disease: Adiposis Dolorosa
Adiposis Dolorosa 		1 0 1 1.6E-03 0 0
CUI: C0001630
Disease: Adrenal Rest Tumor
Adrenal Rest Tumor 		2 0 1 1.6E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 1.6E-03 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 1 1.6E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.5E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 1.6E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		2 0 1 1.6E-03 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 1.6E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 1.6E-03 0 0
CUI: C0002831
Disease: Ancylostomiasis
Ancylostomiasis 		1 0 1 1.6E-03 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		5 0 1 1.6E-03 0 0
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia 		16 0 1 1.5E-03 0 0
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		22 0 1 1.5E-03 0 0
CUI: C0002989
Disease: Epithelioid hemangioma of skin
Epithelioid hemangioma of skin 		5 0 1 1.6E-03 0 0