Source: ALL
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: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.1E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 6 5.4E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 1 4.8E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 3.4E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.9E-02 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 2.0E-02 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 3 1.9E-02 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 3 6.6E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 1 7.5E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma 		1183 0 2 1.7E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		17 0 1 2.6E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 1 9.0E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 1.3E-02 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction 		110 0 2 1.5E-02 0 0
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		218 0 1 4.2E-03 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication 		52 0 2 2.7E-02 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 0 2 3.3E-03 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 1 3.6E-02 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes 		112 0 1 7.5E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 2 3.9E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 2 1.5E-02 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 1 9.3E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		10 0 1 3.1E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 9.3E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.4E-02 0 0