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: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 5.9E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.4E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.2E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 8.9E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 3.6E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 8.5E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.5E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.4E-02 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 1.1E-02 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil 		2 0 1 1.5E-02 0 0
CUI: C0001486
Disease: Adenovirus Infections
Adenovirus Infections 		145 0 1 4.7E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 1.4E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 1.3E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 1.3E-02 0 0
CUI: C0001676
Disease: Adult Antisocial Behavior
Adult Antisocial Behavior 		1 0 1 1.5E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 9.2E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 4.1E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 1.2E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 8.3E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		13 0 1 1.3E-02 0 0
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis 		65 0 1 7.6E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 6.6E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 7.9E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 9.7E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.2E-02 0 0