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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 3 8.7E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 9.2E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 8 7.0E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 3.4E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 2 8.7E-03 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 1 6.5E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 1.8E-02 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 4.9E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
94 0 1 7.2E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
435 0 4 8.4E-03 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
130 0 1 5.7E-03 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
2235 0 9 4.0E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma
1183 0 6 4.9E-03 0 0
CUI: C0001486
Disease: Adenovirus Infections
Adenovirus Infections
145 0 1 5.3E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction
50 0 1 1.1E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms
94 0 1 7.2E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 7.6E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 1.9E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related
89 0 1 7.5E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 2 9.1E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
282 0 1 3.1E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.0E-02 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex
100 0 1 6.9E-03 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction
110 0 1 6.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.1E-02 0 0