Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 4.0E-02
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 4.0E-02
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 1.9E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 1.9E-03 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 1.9E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 1.9E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 1.9E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 1.9E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 1.9E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 1.9E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 1.9E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.8E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease
2 0 1 1.9E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 1.8E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia
2 0 1 1.9E-03 0 0
Amino Acid Metabolism, Inborn Errors
20 0 1 1.9E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia
5 0 1 1.9E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
6 0 1 1.9E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 1.9E-03 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
16 0 1 1.9E-03 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic
1 0 1 1.9E-03 0 0
CUI: C0002985
Disease: Angiokeratoma
Angiokeratoma
4 0 1 1.9E-03 0 0
CUI: C0002992
Disease: Angiomatosis
Angiomatosis
4 0 1 1.9E-03 0 0
CUI: C0002994
Disease: Angioedema
Angioedema
18 0 1 1.9E-03 0 0
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome
21 0 1 1.9E-03 0 0