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: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium 		0 8 0 0 2 8.7E-02
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0 7 0 0 1 4.3E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 4.0E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.9E-02
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 5.0E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 1 2.7E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 4.0E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 5.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.9E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 5.6E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 4.0E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0 14 0 0 2 6.9E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 5.3E-02
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.0E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.5E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.4E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.2E-02 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis 		22 0 1 1.8E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 1.3E-02 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.2E-02 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		11 0 1 2.2E-02 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 2.3E-02 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 1.7E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.4E-02 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 1.8E-02 0 0