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: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 3 1.1E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 2 7.1E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 2 7.3E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 1 5.1E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 3 8.3E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 5 1.1E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 4.1E-03 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 1 4.3E-03 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex 		100 0 2 6.9E-03 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction 		110 0 1 3.3E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 2 8.5E-03 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria 		76 0 3 1.1E-02 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		210 0 3 7.6E-03 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 0 13 1.7E-02 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 5.1E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 4.7E-03 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 1 5.1E-03 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes 		112 0 5 1.7E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 6 8.9E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 1 3.3E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		101 0 2 6.9E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 0 62 1.8E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma 		174 0 4 1.1E-02 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 4.0E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 2 9.6E-03 0 0