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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 6.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 0.12
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 0.12
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 0.12
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 0.11
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.0E-01
CUI: C0000734
Disease: Abdominal mass
Abdominal mass
2 0 1 2.6E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 2.5E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 2.5E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 2.6E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis
4 0 1 2.6E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 2.6E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 2.5E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 2.6E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 2.5E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 2.6E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 1 2.5E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 2.5E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
29 0 1 2.4E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 2.6E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 2.4E-03 0 0
Amino Acid Metabolism, Inborn Errors
20 0 1 2.5E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia
5 0 1 2.6E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
6 0 1 2.6E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity
2 0 1 2.6E-03 0 0