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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.5E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 1.7E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.5E-02
CUI: C0268749
Disease: Fibrillary glomerulonephritis
Fibrillary glomerulonephritis 		0 1 0 0 1 1.7E-02
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 1.7E-02
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 1.7E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.7E-02
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		0 12 0 0 1 1.4E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 1.6E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 1.7E-02
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 1.7E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.6E-02
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute 		2 0 1 5.0E-03 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass 		2 0 1 5.0E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms 		13 0 1 4.8E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 5.0E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 4.8E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 4.9E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma 		11 0 1 4.8E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 4.9E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 5.0E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 4.9E-03 0 0