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: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
29 0 1 3.9E-04 0 0
Hereditary Autosomal Dominant Spastic Paraplegia
27 0 1 3.9E-04 0 0
Increased intramyocellular lipid droplets
27 0 1 3.9E-04 0 0
Autosomal dominant compelling helio ophthalmic outburst syndrome
26 0 1 3.9E-04 0 0
CUI: C4551568
Disease: Joubert syndrome 1
Joubert syndrome 1
26 0 1 3.9E-04 0 0
CUI: C0006325
Disease: Bruxism
Bruxism
24 0 1 4.0E-04 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change
24 0 1 4.0E-04 0 0
Hereditary liability to pressure palsies
23 0 1 4.0E-04 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding)
23 0 1 4.0E-04 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy
23 0 1 4.0E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes
23 0 1 4.0E-04 0 0
CUI: C0085610
Disease: Sinus bradycardia
Sinus bradycardia
22 0 1 4.0E-04 0 0
CUI: C4021657
Disease: Abnormality of bone mineral density
Abnormality of bone mineral density
22 0 1 4.0E-04 0 0
Parkinsonism with favorable response to dopaminergic medication
21 0 1 4.0E-04 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram
21 0 1 4.0E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum
21 0 1 4.0E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin
21 0 1 4.0E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia
21 0 1 4.0E-04 0 0
Total iron binding capacity function
20 0 1 4.0E-04 0 0
Iron binding capacity total measurement
20 0 1 4.0E-04 0 0
CUI: C1963175
Disease: Sinus Bradycardia, CTCAE
Sinus Bradycardia, CTCAE
20 0 1 4.0E-04 0 0
continuous electrocardiogram sinus bradycardia (finding)
20 0 1 4.0E-04 0 0
Juvenile amyotrophic lateral sclerosis
20 0 1 4.0E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes
19 0 1 4.0E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease
19 0 1 4.0E-04 0 0