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 9.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.33
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 35 0 0 1 2.7E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 8.0E-03
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 0.20
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.33
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.33
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 9.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 0.20
CUI: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 1.1E-02 0 0
CUI: C0006015
Disease: Bordetella Infections
Bordetella Infections 		1 0 1 1.1E-02 0 0
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 1.1E-02 0 0
CUI: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		1 0 1 1.1E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 1.1E-02 0 0
CUI: C0013505
Disease: Echinococcosis, Pulmonary
Echinococcosis, Pulmonary 		1 0 1 1.1E-02 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 1.1E-02 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 1.1E-02 0 0
CUI: C0024588
Disease: Malignant essential hypertension
Malignant essential hypertension 		1 0 1 1.1E-02 0 0
CUI: C0025464
Disease: Mesenchymoma
Mesenchymoma 		1 0 1 1.1E-02 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 1.1E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 1.1E-02 0 0
CUI: C0039870
Disease: Thinness
Thinness 		1 0 1 1.1E-02 0 0
CUI: C0040409
Disease: Tongue Diseases
Tongue Diseases 		1 0 1 1.1E-02 0 0
CUI: C0042548
Disease: Plantar wart
Plantar wart 		1 0 1 1.1E-02 0 0
CUI: C0085438
Disease: Meningitis, Fungal
Meningitis, Fungal 		1 0 1 1.1E-02 0 0