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: C1868414
Disease: HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO 		1 0 1 1.00 0 0
CUI: C3854611
Disease: Anticipatory nausea
Anticipatory nausea 		2 0 1 0.50 0 0
CUI: C1387528
Disease: Acute haemolytic anaemia
Acute haemolytic anaemia 		3 0 1 0.33 0 0
CUI: C0151620
Disease: Hypertensive Encephalopathy
Hypertensive Encephalopathy 		4 0 1 0.25 0 0
CUI: C0264802
Disease: Dilated cardiomyopathy secondary to metabolic disorder
Dilated cardiomyopathy secondary to metabolic disorder 		5 0 1 0.20 0 0
CUI: C1323099
Disease: sympathomimetic disorder
sympathomimetic disorder 		6 0 1 0.17 0 0
CUI: C2047520
Disease: Mixed hyperlipidemia (disorder)
Mixed hyperlipidemia (disorder) 		6 0 1 0.17 0 0
CUI: C3827253
Disease: Classical Glioblastoma
Classical Glioblastoma 		6 0 1 0.17 0 0
CUI: C2936846
Disease: Scarring alopecia
Scarring alopecia 		8 0 1 0.12 0 0
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		9 0 1 0.11 0 0
CUI: C0205822
Disease: Hibernoma
Hibernoma 		10 0 1 1.0E-01 0 0
CUI: C0581384
Disease: Chronic anemia
Chronic anemia 		10 0 1 1.0E-01 0 0
CUI: C1281300
Disease: Vascular degeneration
Vascular degeneration 		10 0 1 1.0E-01 0 0
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		10 0 1 1.0E-01 0 0
CUI: C0023645
Disease: Lichen planus follicularis
Lichen planus follicularis 		13 0 1 7.7E-02 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 1 7.1E-02 0 0
CUI: C1863844
Disease: Adult-onset citrullinemia type 2
Adult-onset citrullinemia type 2 		14 0 1 7.1E-02 0 0
CUI: C4045968
Disease: Altitude Hypoxia
Altitude Hypoxia 		14 0 1 7.1E-02 0 0
CUI: C3887523
Disease: Very long chain acyl-CoA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency 		15 0 1 6.7E-02 0 0
CUI: C0396060
Disease: Congenital laryngeal adductor palsy
Congenital laryngeal adductor palsy 		17 0 1 5.9E-02 0 0
CUI: C0948908
Disease: Nephrotoxic serum nephritis
Nephrotoxic serum nephritis 		17 0 1 5.9E-02 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		17 0 1 5.9E-02 0 0
CUI: C0334409
Disease: Leydig cell tumor, benign
Leydig cell tumor, benign 		18 0 1 5.6E-02 0 0
CUI: C1706412
Disease: Lipidemias
Lipidemias 		18 0 1 5.6E-02 0 0
CUI: C0027441
Disease: Nasopharyngitis
Nasopharyngitis 		19 0 1 5.3E-02 0 0