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: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 2.1E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.0E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.0E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 3.5E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 1 4.5E-03 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 1 7.0E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess
96 0 1 7.7E-03 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis
22 0 1 1.8E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 1.3E-02 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
94 0 1 7.8E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 1 2.4E-02 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma
21 0 1 1.8E-02 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 2.3E-02 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction
50 0 1 1.2E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
90 0 1 8.1E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 8.3E-03 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related
89 0 1 8.1E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 4.8E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.1E-02 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction
110 0 1 6.9E-03 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication
52 0 1 1.2E-02 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria
13 0 1 2.1E-02 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
114 0 1 6.8E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss
101 0 1 7.4E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta
61 0 1 1.1E-02 0 0