Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 3.0E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 3.0E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 6.1E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 3.0E-03
CUI: C0429908
Disease: Susceptibility to tuberculosis
Susceptibility to tuberculosis
0 1 0 0 1 3.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 3.0E-03
Multi vessel coronary artery disease
0 1 0 0 1 3.0E-03
Peroxisome Biogenesis Disorder, Complementation Group C
0 2 0 0 1 3.0E-03
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 3.0E-03
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 3.0E-03
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 3.0E-03
Diabetic peripheral neuropathic pain
0 1 0 0 1 3.0E-03
CUI: C3280647
Disease: BACTEREMIA, SUSCEPTIBILITY TO, 2
BACTEREMIA, SUSCEPTIBILITY TO, 2
0 1 0 0 1 3.0E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 3.0E-03
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 3.0E-03
CUI: C0011053
Disease: Deafness
Deafness
62 0 1 7.6E-04 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
57 0 1 7.6E-04 0 0
Adverse effects, not elsewhere classified
55 0 1 7.6E-04 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 7.6E-04 0 0
Increased variability in muscle fiber diameter
50 0 1 7.7E-04 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux
50 0 1 7.7E-04 0 0
CUI: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea
49 0 1 7.7E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus
48 0 1 7.7E-04 0 0
CUI: C0581342
Disease: Redundant skin
Redundant skin
48 0 1 7.7E-04 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High
47 0 1 7.7E-04 0 0