Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION
1 0 1 3.8E-02 0 0
CUI: C4531226
Disease: Abnormal perifollicular morphology
Abnormal perifollicular morphology
1 0 1 3.8E-02 0 0
CUI: C4552078
Disease: PSEUDO-TORCH SYNDROME 1
PSEUDO-TORCH SYNDROME 1
1 0 1 3.8E-02 0 0
CUI: C0022906
Disease: Lacrimal Duct Obstruction
Lacrimal Duct Obstruction
2 0 1 3.7E-02 0 0
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders
2 0 1 3.7E-02 0 0
CUI: C0157742
Disease: Urticaria due to cold and heat
Urticaria due to cold and heat
2 0 1 3.7E-02 0 0
CUI: C0263778
Disease: Chronic osteoarthritis
Chronic osteoarthritis
2 0 1 3.7E-02 0 0
CUI: C0275550
Disease: Acute bacterial peritonitis
Acute bacterial peritonitis
2 0 1 3.7E-02 0 0
CUI: C0276035
Disease: Glasser's disease
Glasser's disease
2 0 1 3.7E-02 0 0
CUI: C0332477
Disease: Erythematous plaque
Erythematous plaque
2 0 1 3.7E-02 0 0
CUI: C0334416
Disease: Parasympathetic paraganglioma
Parasympathetic paraganglioma
2 0 1 3.7E-02 0 0
Familial non-neuropathic amyloidosis
2 0 1 3.7E-02 0 0
CUI: C0406097
Disease: Streptococcal impetigo
Streptococcal impetigo
2 0 1 3.7E-02 0 0
CUI: C0406653
Disease: Eosinophilic spongiosis
Eosinophilic spongiosis
2 0 1 3.7E-02 0 0
Junctional epidermolysis bullosa mitis
2 0 1 3.7E-02 0 0
CUI: C0474819
Disease: Glomus vagale tumor
Glomus vagale tumor
2 0 1 3.7E-02 0 0
CUI: C0543673
Disease: Fibrinolytic disorder
Fibrinolytic disorder
2 0 1 3.7E-02 0 0
CUI: C0747739
Disease: polyglandular failure
polyglandular failure
2 0 1 3.7E-02 0 0
Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related
2 0 1 3.7E-02 0 0
HIV-1-Associated Cognitive Motor Complex
2 0 1 3.7E-02 0 0
CUI: C1274789
Disease: Ligneous conjunctivitis
Ligneous conjunctivitis
2 0 1 3.7E-02 0 0
CUI: C1304249
Disease: Cutaneous xanthoma
Cutaneous xanthoma
2 0 1 3.7E-02 0 0
Invasive Group A beta-hemolytic streptococcal disease
2 0 1 3.7E-02 0 0
Undifferentiated inflammatory arthritis
2 0 1 3.7E-02 0 0
CUI: C1719313
Disease: Hereditary amyloid nephropathy
Hereditary amyloid nephropathy
2 0 1 3.7E-02 0 0