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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.0E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.1E-02
CUI: C3714987
Disease: BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17 		0 1 0 0 1 1.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.1E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 1.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.1E-02
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.1E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 2.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 2.2E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 2.2E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 2.2E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 2.2E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil 		2 0 1 2.2E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 2.1E-03 2 2.1E-02
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases 		3 0 1 2.2E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		17 0 1 2.1E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 2.2E-03 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium 		23 0 1 2.1E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 2.2E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.1E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 2.2E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 2.2E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 2.1E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 2.2E-03 0 0