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 2.0E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 2.4E-02
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 2.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 2.4E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.4E-02
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 2.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 2.3E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 2.3E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 2.3E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 2.3E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 2.3E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 2.3E-03 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis
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: C0001249
Disease: Actinobacillus Infections
Actinobacillus Infections
1 0 1 2.3E-03 0 0
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
Acute vascular insufficiency of intestine (disorder)
8 0 1 2.3E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 2.3E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 1 2.2E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 2.3E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 2.1E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease
2 0 1 2.3E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 2.2E-03 0 0