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 3.2E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 2 1.8E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 2 7.7E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 5.8E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.3E-02 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
94 0 1 9.5E-03 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
243 0 1 3.9E-03 0 0
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease
35 0 1 2.2E-02 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
130 0 3 2.2E-02 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
2 0 1 7.7E-02 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 1 8.2E-03 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
2235 0 8 3.6E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma
1183 0 3 2.5E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 2 6.1E-02 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
282 0 1 3.4E-03 0 0
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder
218 0 1 4.4E-03 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
577 0 1 1.7E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis
13 0 1 4.2E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia
491 0 5 1.0E-02 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
114 0 1 8.0E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss
101 0 2 1.8E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 8 2.4E-03 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
694 0 2 2.8E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1114 0 2 1.8E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
14 0 1 4.0E-02 0 0