Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Benign paroxysmal vertigo of childhood
0 1 0 0 1 7.1E-02
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 1 9.0E-04 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 3.2E-02 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
435 0 1 2.3E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma
1183 0 1 8.4E-04 0 0
CUI: C0001618
Disease: Tumors of Adrenal Cortex
Tumors of Adrenal Cortex
74 0 1 1.2E-02 0 0
CUI: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal
7 0 1 6.2E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
85 0 1 1.1E-02 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
694 0 1 1.4E-03 0 0
CUI: C0002793
Disease: Anaplasia
Anaplasia
538 0 1 1.8E-03 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
154 0 1 6.1E-03 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 1 2.3E-03 0 0
CUI: C0002949
Disease: Aneurysm, Dissecting
Aneurysm, Dissecting
33 0 1 2.4E-02 0 0
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
840 0 1 1.2E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation
88 0 1 1.0E-02 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: C0003537
Disease: Aphasia
Aphasia
86 0 1 1.1E-02 0 0
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: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 4.8E-03 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
384 0 1 2.5E-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