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: C0265514
Disease: Dermatofibrosis lenticularis disseminata
Dermatofibrosis lenticularis disseminata 		0 3 0 0 1 2.2E-03
CUI: C0276340
Disease: Respiratory syncytial virus bronchiolitis
Respiratory syncytial virus bronchiolitis 		0 1 0 0 1 2.2E-03
CUI: C0947912
Disease: Myasthenias
Myasthenias 		0 3 0 0 1 2.2E-03
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.9E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 2.9E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 2.5E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 2.8E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 2.7E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 2.9E-03 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 2.8E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 2.9E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 2.9E-03 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 1 2.9E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction 		50 0 1 2.6E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 2.6E-03 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 1 2.6E-03 0 0
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction 		110 0 1 2.2E-03 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria 		76 0 1 2.4E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		13 0 1 2.9E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 1 2.4E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 2.4E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 2.5E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 2.7E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.8E-03 0 0
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		24 0 1 2.8E-03 0 0