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 1 8.1E-03 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 3 2.4E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 2 1.7E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 1.3E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 3 2.5E-02 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 4 1.9E-02 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 2 6.3E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 2.0E-02 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 1 1.3E-02 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex 		100 0 1 7.5E-03 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication 		52 0 1 1.2E-02 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 0 2 3.3E-03 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 2.3E-02 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 1.7E-02 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes 		112 0 1 6.8E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 5 9.6E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 1 8.3E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		101 0 3 2.3E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 0 15 4.4E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 2 1.7E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma 		174 0 5 2.5E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.9E-02 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		694 0 3 4.1E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		1114 0 6 5.2E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 2.1E-02 0 0