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: C0002991
Disease: Cutaneous Fibrous Histiocytoma
Cutaneous Fibrous Histiocytoma 		42 0 1 1.1E-02 0 0
CUI: C0003076
Disease: Aniridia
Aniridia 		83 0 1 7.6E-03 0 0
CUI: C0003079
Disease: Anisocoria
Anisocoria 		7 5 1 1.8E-02 1 1.6E-02
CUI: C0003081
Disease: Anisometropia
Anisometropia 		7 0 1 1.8E-02 0 0
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		202 0 1 4.0E-03 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 1 1.1E-02 0 0
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm 		278 0 1 3.1E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency 		377 0 1 2.3E-03 0 0
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		234 0 1 3.5E-03 0 0
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		163 0 1 4.7E-03 0 0
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		206 0 1 3.9E-03 0 0
CUI: C0003869
Disease: Arthritis, Infectious
Arthritis, Infectious 		33 0 1 1.2E-02 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		450 0 1 2.0E-03 0 0
CUI: C0003962
Disease: Ascites
Ascites 		198 0 1 4.0E-03 0 0
CUI: C0004099
Disease: Asthma, Exercise-Induced
Asthma, Exercise-Induced 		8 3 1 1.8E-02 2 3.4E-02
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 1 1.2E-02 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis 		62 2 1 9.0E-03 2 3.4E-02
CUI: C0004269
Disease: Child attention deficit disorder
Child attention deficit disorder 		26 0 1 1.3E-02 0 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		70 0 1 8.4E-03 0 0
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities 		16 0 1 1.5E-02 0 0
CUI: C0004565
Disease: Melanoma, B16
Melanoma, B16 		157 0 1 4.9E-03 0 0
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections 		616 0 1 1.5E-03 0 0
CUI: C0004698
Disease: Balkan Nephropathy
Balkan Nephropathy 		34 0 1 1.2E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 1 1.5E-02 0 0
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		107 0 1 6.4E-03 0 0