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 1 3.1E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 3 2.7E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 3.7E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
435 0 1 2.2E-03 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
2235 0 2 8.9E-04 0 0
CUI: C0001430
Disease: Adenoma
Adenoma
1183 0 1 8.3E-04 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 9.6E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
43 0 1 1.7E-02 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 5.2E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
282 0 1 3.3E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.4E-02 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex
100 0 1 8.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.6E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.1E-02 0 0
CUI: C0002020
Disease: Alexithymia
Alexithymia
39 0 1 1.8E-02 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes
112 0 1 7.8E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia
491 0 3 5.9E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 4 1.2E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
85 0 1 9.8E-03 0 0
CUI: C0002622
Disease: Amnesia
Amnesia
173 0 1 5.3E-03 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
694 0 1 1.4E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1114 0 1 8.8E-04 0 0
CUI: C0002792
Disease: anaphylaxis
anaphylaxis
180 0 1 5.1E-03 0 0
CUI: C0002793
Disease: Anaplasia
Anaplasia
538 0 2 3.6E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 0 4 4.6E-03 0 0