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: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 5 7.9E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
231 0 37 5.1E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
237 0 14 1.9E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
58 0 3 5.1E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
38 0 9 1.6E-02 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 1.8E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
9 0 1 1.9E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
167 0 16 2.3E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
22 0 5 9.1E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
11 0 1 1.8E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
6 0 1 1.9E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
35 0 15 2.7E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
19 0 1 1.8E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 8 1.1E-02 0 0
CUI: C0001811
Disease: Aging
Aging
1 0 1 1.9E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
11 0 1 1.8E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 1.8E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
19 0 1 1.8E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
76 0 3 5.0E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea
29 0 1 1.8E-03 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
6 0 1 1.9E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
78 0 3 4.9E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia
308 0 15 1.8E-02 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
63 0 3 5.1E-03 0 0
CUI: C0002880
Disease: Autoimmune hemolytic anemia
Autoimmune hemolytic anemia
26 0 1 1.8E-03 0 0