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 1.0E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.0E-02
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 2.1E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.0E-02
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 1.0E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.0E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.0E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.0E-02
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 2.4E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 2.4E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 2.5E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.5E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 2.5E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.5E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 2.5E-03 0 0
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases 		3 0 1 2.6E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 2.5E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 1 2.5E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 2.4E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 2.5E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		10 0 1 2.5E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 2.4E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.5E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 2.5E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 2.6E-03 0 0