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 1.9E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.2E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.2E-02
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms 		13 0 1 1.8E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.8E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 1.8E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.8E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 1.8E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 1.8E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.8E-03 0 0
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases 		3 0 1 1.8E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 1.8E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 1.8E-03 0 0
CUI: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases 		1 0 1 1.8E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 1.7E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 1.8E-03 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 1.8E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 1.8E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 1.7E-03 0 0
CUI: C0002623
Disease: Post-traumatic amnesia
Post-traumatic amnesia 		9 0 1 1.8E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 1.8E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 1.8E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		2 0 1 1.8E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 1.8E-03 0 0