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: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 2.9E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 2.9E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 2.6E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 2.9E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 2.8E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 2.9E-03 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 2.9E-03 0 0
Herpetic Acute Necrotizing Encephalitis
5 0 1 2.9E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
2 0 1 3.0E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 2.9E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 2.9E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 2.9E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 2.9E-03 0 0
CUI: C0001752
Disease: African swine fever
African swine fever
1 0 1 3.0E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease
2 0 1 3.0E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria
13 0 1 2.9E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta
61 0 1 2.5E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea
37 0 1 2.7E-03 0 0
Amino Acid Metabolism, Inborn Errors
20 0 1 2.8E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia
5 0 1 2.9E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
6 0 1 2.9E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity
2 0 1 3.0E-03 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease
2 0 1 3.0E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 3.0E-03 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired
16 0 1 2.8E-03 0 0