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 6.0E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 6.0E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.0E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 6.0E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 5.9E-03
CUI: C1876181
Disease: EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS 		0 2 0 0 1 5.9E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 6.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 5.9E-03
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 5.6E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.0E-03
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 6.0E-03
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.1E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 1.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 1.1E-03 0 0
CUI: C0001249
Disease: Actinobacillus Infections
Actinobacillus Infections 		1 0 1 1.1E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 1.1E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 1.1E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 1.1E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.1E-03 0 0
CUI: C0001432
Disease: Adenoma, Chromophobe
Adenoma, Chromophobe 		1 0 1 1.1E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 1.1E-03 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 1.1E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 1.1E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 1.1E-03 0 0