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: C0400807
Disease: Stress ulcer of stomach
Stress ulcer of stomach 		14 0 6 7.4E-02 0 0
CUI: C2741638
Disease: Stress ulcer
Stress ulcer 		14 0 6 7.4E-02 0 0
CUI: C4025249
Disease: Abnormality of the intervertebral disk
Abnormality of the intervertebral disk 		30 0 7 7.3E-02 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 6 7.1E-02 0 0
CUI: C1279296
Disease: Chronic leukemia (category)
Chronic leukemia (category) 		32 0 7 7.1E-02 0 0
CUI: C0035288
Disease: Reticuloendotheliosis, X-linked
Reticuloendotheliosis, X-linked 		48 0 8 7.1E-02 0 0
CUI: C0013370
Disease: Amebic colitis
Amebic colitis 		49 0 8 7.0E-02 0 0
CUI: C0013604
Disease: Edema
Edema 		126 0 13 7.0E-02 0 0
CUI: C0178664
Disease: Glomerulosclerosis (disorder)
Glomerulosclerosis (disorder) 		221 0 19 6.9E-02 0 0
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis 		129 0 13 6.9E-02 0 0
CUI: C0233746
Disease: Perceptual disturbance
Perceptual disturbance 		5 0 5 6.8E-02 0 0
CUI: C0002438
Disease: Amebiasis
Amebiasis 		37 0 7 6.8E-02 0 0
CUI: C0021151
Disease: Incipient Schizophrenia
Incipient Schizophrenia 		6 0 5 6.8E-02 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 1 5 6.8E-02 1 4.0E-02
CUI: C0730315
Disease: Acute central serous chorioretinopathy
Acute central serous chorioretinopathy 		7 0 5 6.7E-02 0 0
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy 		55 0 8 6.7E-02 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 5 6.7E-02 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 7 6.7E-02 0 0
CUI: C3495949
Disease: Locally advanced breast cancer
Locally advanced breast cancer 		71 0 9 6.7E-02 0 0
CUI: C0878552
Disease: Coronary artery ectasia
Coronary artery ectasia 		24 0 6 6.6E-02 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 10 6.6E-02 0 0
CUI: C0030779
Disease: Pelger-Huet Anomaly
Pelger-Huet Anomaly 		25 0 6 6.5E-02 0 0
CUI: C0375019
Disease: Human T-cell lymphotrophic virus, type I [HTLV-I]
Human T-cell lymphotrophic virus, type I [HTLV-I] 		25 0 6 6.5E-02 0 0
CUI: C0746883
Disease: Febrile Neutropenia
Febrile Neutropenia 		58 0 8 6.5E-02 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 7 6.5E-02 0 0