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 5.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.4E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 5.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 5.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 5.3E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 5.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 1.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 1.6E-02
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.3E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 1.3E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.3E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.3E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 1.3E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 1.3E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 1 1.3E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 1.3E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 1.3E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.3E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 1.3E-03 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 1.3E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 1.3E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 1.3E-03 0 0
CUI: C0002831
Disease: Ancylostomiasis
Ancylostomiasis 		1 0 1 1.3E-03 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		5 0 1 1.3E-03 0 0