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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.2E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 1.2E-02
Juvenile idiopathic arthritis, enthesitis related arthritis
0 1 0 0 1 1.2E-02
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO
0 3 0 0 2 2.4E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.2E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 2.3E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 2.3E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 2.3E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 2.3E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 2.4E-03 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 3 1 2.3E-03 1 1.2E-02
Herpetic Acute Necrotizing Encephalitis
5 0 1 2.3E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
2 0 1 2.3E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 2.3E-03 0 0
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases
3 0 1 2.3E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 2.3E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 2.1E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 2.2E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
85 0 1 2.0E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia
2 0 1 2.3E-03 0 0
Amino Acid Metabolism, Inborn Errors
20 0 1 2.3E-03 0 0
CUI: C0002623
Disease: Post-traumatic amnesia
Post-traumatic amnesia
9 0 1 2.3E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia
5 0 1 2.3E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity
2 0 1 2.3E-03 0 0