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: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 2 0.13
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 4.8E-02
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases 		0 7 0 0 1 5.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 7.7E-02
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 7.7E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer 		0 2 0 0 1 7.1E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 5.9E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.4E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 144 0 0 1 6.4E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 7.1E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon 		0 1 0 0 1 7.7E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 4.0E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 4.8E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 7.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 6.7E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 7.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 7.7E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 7.1E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 7.7E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 4.8E-02
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		0 36 0 0 1 2.1E-02
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
Large-artery atherosclerosis (embolus/thrombosis) 		0 35 0 0 1 2.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 6.7E-02
CUI: C0003944
Disease: As If Personality
As If Personality 		1 0 1 3.0E-02 0 0
CUI: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 3.0E-02 0 0