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: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 2 6.3E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 3 2.7E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 4 3.7E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 1.5E-02 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		94 0 3 2.8E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 1 3.9E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 3 2.0E-02 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 1 2.2E-03 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		130 0 2 1.4E-02 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 3 0.14 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 2 1.6E-02 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		2235 0 6 2.7E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma 		1183 0 4 3.3E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 2 2.0E-02 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 2 6.8E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 2 2.9E-02 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication 		52 0 1 1.5E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 2 4.0E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 1 7.8E-03 0 0
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis 		65 0 1 1.3E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 0 9 2.6E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 1.0E-02 0 0
CUI: C0002438
Disease: Amebiasis
Amebiasis 		37 0 2 3.9E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.9E-02 0 0
CUI: C0002622
Disease: Amnesia
Amnesia 		173 0 1 5.3E-03 0 0