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: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 5.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 7.4E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 6.9E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 7.2E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 7.0E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 7.1E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 6.5E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 7.0E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction 		50 0 1 5.5E-03 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 1 4.5E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 5.7E-03 0 0
CUI: C0001811
Disease: Aging
Aging 		1 0 1 7.5E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 6.7E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		29 0 1 6.2E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 5.6E-03 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium 		23 0 1 6.4E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 1 4.6E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 4.6E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 7.4E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 5.9E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 7.2E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 7.2E-03 0 0
CUI: C0002690
Disease: Amputation Stumps
Amputation Stumps 		11 0 1 6.9E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 6.8E-03 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		16 0 1 6.7E-03 0 0