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: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 1 3.1E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 4 1.3E-02 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		23 0 1 3.9E-03 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 1 3.1E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.4E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 4 1.4E-02 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 3 1.1E-02 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex 		100 0 4 1.2E-02 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction 		110 0 2 5.8E-03 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication 		52 0 1 3.5E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 3.9E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		13 0 1 4.1E-03 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes 		112 0 8 2.4E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 13 1.8E-02 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 8 2.4E-02 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 6 1.9E-02 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		10 0 2 8.3E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		101 0 2 6.0E-03 0 0
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis 		65 0 2 6.7E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 3.1E-03 0 0
CUI: C0002438
Disease: Amebiasis
Amebiasis 		37 0 1 3.7E-03 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma 		174 0 3 7.4E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 3.4E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 2 7.4E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 4.0E-03 0 0