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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 1.5E-02
CUI: C0034882
Disease: Rectal Diseases
Rectal Diseases 		0 3 0 0 1 1.5E-02
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 1.5E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.4E-02
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0 69 0 0 1 7.5E-03
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.2E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 2.2E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 2.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 2.2E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.1E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 2.2E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.2E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 2.2E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 2.2E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 2.2E-03 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 2.2E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 2.1E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 2.1E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 2.2E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 2.0E-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