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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.5E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 6.5E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.5E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 6.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 6.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.5E-03
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 6.5E-03
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 1.1E-03 0 0
CUI: C0001139
Disease: Acinetobacter Infections
Acinetobacter Infections 		1 0 1 1.2E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 1.2E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.2E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 1.2E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 1.2E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil 		2 0 1 1.2E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 1.2E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 1.2E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 1 1.2E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 1.2E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 1.2E-03 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 1.2E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.1E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 1.2E-03 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		5 0 1 1.2E-03 0 0
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 0 1 1.2E-03 0 0