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 8.0E-03 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass 		2 0 1 4.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 6 1.9E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 3 2.7E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 8.5E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 5.5E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 2 8.7E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 2.4E-02 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 6.3E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 4.2E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 2 6.9E-02 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		2235 0 8 3.6E-03 0 0
CUI: C0001430
Disease: Adenoma
Adenoma 		1183 0 6 5.0E-03 0 0
CUI: C0001618
Disease: Tumors of Adrenal Cortex
Tumors of Adrenal Cortex 		74 0 1 1.0E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 3.2E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 3 2.6E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 4 3.8E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 1.5E-02 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 2 6.6E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 1.3E-02 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 0 1 1.7E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 2 3.9E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 0 8 2.3E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 1.2E-02 0 0
CUI: C0002622
Disease: Amnesia
Amnesia 		173 0 2 1.0E-02 0 0