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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.0E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 4.9E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
282 0 1 3.2E-03 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
577 0 1 1.7E-03 0 0
CUI: C0002020
Disease: Alexithymia
Alexithymia
39 0 1 1.5E-02 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss
101 0 1 7.7E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
85 0 1 8.8E-03 0 0
CUI: C0002873
Disease: Anemia of chronic disease
Anemia of chronic disease
100 0 1 7.8E-03 0 0
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
238 0 1 3.7E-03 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 1 2.2E-03 0 0
CUI: C0002991
Disease: Cutaneous Fibrous Histiocytoma
Cutaneous Fibrous Histiocytoma
42 0 1 1.4E-02 0 0
CUI: C0003165
Disease: Anthracosis
Anthracosis
65 0 1 1.1E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 6.0E-03 0 0
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm
278 0 1 3.3E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
377 0 1 2.5E-03 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
559 0 1 1.7E-03 0 0
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula
93 0 1 8.2E-03 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia
248 0 1 3.6E-03 0 0
CUI: C0003864
Disease: Arthritis
Arthritis
1072 0 1 9.1E-04 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma
985 0 1 9.9E-04 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 1.1E-02 0 0
CUI: C0004158
Disease: Athetosis
Athetosis
39 0 1 1.5E-02 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
1758 0 1 5.6E-04 0 0
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections
616 0 1 1.6E-03 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
502 0 1 1.9E-03 0 0