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 3.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 4.5E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0 220 0 0 1 4.1E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 4.5E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0 19 0 0 1 2.5E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 4.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.5E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 4.2E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 9.1E-02
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 3.3E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 3.4E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 3.4E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 3.2E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 3.4E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 3.4E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 3.4E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma 		11 0 1 3.4E-03 0 0
CUI: C0001432
Disease: Adenoma, Chromophobe
Adenoma, Chromophobe 		1 0 1 3.5E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 3.4E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 3.4E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 3.3E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 3.3E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 3.4E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		2 0 1 3.5E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 3.3E-03 0 0