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: C0026471
Disease: Monoclonal paraproteinemia
Monoclonal paraproteinemia
0 1 0 0 1 0.14
CUI: C0221030
Disease: Hyperviscosity syndrome
Hyperviscosity syndrome
0 1 0 0 1 0.14
CUI: C0270710
Disease: Bing-Neel syndrome
Bing-Neel syndrome
0 1 0 0 1 0.14
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen
0 2 0 0 2 0.29
CUI: C0472817
Disease: WHIM syndrome
WHIM syndrome
0 7 0 0 1 7.7E-02
CUI: C1262216
Disease: IgM gammopathy
IgM gammopathy
0 1 0 0 1 0.14
Familial Waldenstrom's Macroglobulinaemia
0 1 0 0 1 0.14
CUI: C4732837
Disease: Leptomeningeal enhancement
Leptomeningeal enhancement
0 1 0 0 1 0.14
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 5.3E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 5.2E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
28 0 1 4.8E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 4.3E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 5.2E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 5.4E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 5.3E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
2 0 1 5.5E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 5.3E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 4.4E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 4.9E-03 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory
6 0 1 5.3E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness
10 0 1 5.2E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
14 0 1 5.1E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 5.5E-03 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired
16 0 1 5.1E-03 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital
27 0 1 4.8E-03 0 0