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: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		840 0 3 3.5E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency 		377 0 1 2.6E-03 0 0
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		234 0 1 4.1E-03 0 0
CUI: C0003578
Disease: Apnea
Apnea 		262 0 1 3.7E-03 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 1 1.3E-02 0 0
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		2006 0 1 5.0E-04 0 0
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		163 0 1 5.8E-03 0 0
CUI: C0003864
Disease: Arthritis
Arthritis 		1072 0 1 9.3E-04 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		450 0 1 2.2E-03 0 0
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		2723 0 2 7.3E-04 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 1 4.9E-03 0 0
CUI: C0004096
Disease: Asthma
Asthma 		2096 0 1 4.8E-04 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 6.4E-03 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		985 0 2 2.0E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 2 2.3E-03 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		384 0 2 5.1E-03 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 1 2.3E-02 0 0
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		2044 0 1 4.9E-04 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		939 0 1 1.1E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		1112 0 1 8.9E-04 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		1758 0 2 1.1E-03 0 0
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections 		616 0 1 1.6E-03 0 0
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		478 0 1 2.1E-03 0 0
CUI: C0004779
Disease: Basal Cell Nevus Syndrome
Basal Cell Nevus Syndrome 		74 0 1 1.2E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 2 7.7E-02 0 0