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: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 6.8E-03 0 0
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease 		35 0 1 2.2E-02 0 0
CUI: C0001486
Disease: Adenovirus Infections
Adenovirus Infections 		145 0 1 6.5E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 1.9E-02 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 1 3.4E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 3.7E-02 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction 		110 0 1 8.3E-03 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication 		52 0 1 1.6E-02 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes 		112 0 1 8.2E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 1 1.0E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma 		174 0 1 5.4E-03 0 0
CUI: C0002622
Disease: Amnesia
Amnesia 		173 0 1 5.5E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		1114 0 1 8.9E-04 0 0
CUI: C0002792
Disease: anaphylaxis
anaphylaxis 		180 0 1 5.3E-03 0 0
CUI: C0002893
Disease: Refractory anemias
Refractory anemias 		340 0 1 2.9E-03 0 0
CUI: C0002894
Disease: Refractory anaemia with excess blasts
Refractory anaemia with excess blasts 		49 0 1 1.7E-02 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		1 0 1 9.1E-02 0 0
CUI: C0002991
Disease: Cutaneous Fibrous Histiocytoma
Cutaneous Fibrous Histiocytoma 		42 0 1 1.9E-02 0 0
CUI: C0003076
Disease: Aniridia
Aniridia 		83 0 1 1.1E-02 0 0
CUI: C0003081
Disease: Anisometropia
Anisometropia 		7 0 1 5.9E-02 0 0
CUI: C0003130
Disease: Anoxia
Anoxia 		287 0 1 3.4E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency 		377 0 1 2.6E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		86 0 1 1.0E-02 0 0
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		163 0 1 5.8E-03 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		450 0 1 2.2E-03 0 0