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: C0017531
Disease: Angiolymphoid hyperplasia
Angiolymphoid hyperplasia
22 0 4 7.7E-02 0 0
CUI: C0085311
Disease: Diffuse cutaneous leishmaniasis
Diffuse cutaneous leishmaniasis
22 0 4 7.7E-02 0 0
CUI: C0086196
Disease: Eczema, Infantile
Eczema, Infantile
36 0 5 7.7E-02 0 0
CUI: C0154307
Disease: Banti's syndrome
Banti's syndrome
8 0 3 7.7E-02 0 0
CUI: C0744471
Disease: Gram-negative bacteremia
Gram-negative bacteremia
8 0 3 7.7E-02 0 0
CUI: C1290638
Disease: Resorption of apex of tooth root
Resorption of apex of tooth root
8 0 3 7.7E-02 0 0
Chronic Prostatitis with Chronic Pelvic Pain Syndrome
8 0 3 7.7E-02 0 0
CUI: C4316791
Disease: Entamoeba histolytica Infection
Entamoeba histolytica Infection
8 0 3 7.7E-02 0 0
CUI: C0025229
Disease: Melioidosis
Melioidosis
65 0 7 7.6E-02 0 0
CUI: C0031046
Disease: Pericarditis
Pericarditis
51 0 6 7.6E-02 0 0
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica
51 0 6 7.6E-02 0 0
CUI: C0036983
Disease: Septic Shock
Septic Shock
37 0 5 7.6E-02 0 0
CUI: C0278147
Disease: Radicular pain
Radicular pain
23 0 4 7.5E-02 0 0
CUI: C2348101
Disease: Destructive Arthritis
Destructive Arthritis
23 0 4 7.5E-02 0 0
CUI: C0162669
Disease: Pleoconial Myopathies
Pleoconial Myopathies
9 0 3 7.5E-02 0 0
CUI: C0949496
Disease: Luft Disease
Luft Disease
9 0 3 7.5E-02 0 0
CUI: C1260710
Disease: Acute ulcerative colitis
Acute ulcerative colitis
9 0 3 7.5E-02 0 0
CUI: C1619727
Disease: Decompensated cirrhosis of liver
Decompensated cirrhosis of liver
52 0 6 7.5E-02 0 0
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
9 0 3 7.5E-02 0 0
CUI: C3698407
Disease: Peri-implant mucositis
Peri-implant mucositis
9 0 3 7.5E-02 0 0
CUI: C3873491
Disease: Invasive meningococcal disease
Invasive meningococcal disease
9 0 3 7.5E-02 0 0
CUI: C0456103
Disease: Sepsis of the newborn
Sepsis of the newborn
53 0 6 7.4E-02 0 0
CUI: C0747256
Disease: Parasitic infection
Parasitic infection
39 0 5 7.4E-02 0 0
CUI: C0162668
Disease: Megaconial Myopathies
Megaconial Myopathies
10 0 3 7.3E-02 0 0
STRIATONIGRAL DEGENERATION, INFANTILE (disorder)
10 0 3 7.3E-02 0 0