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: C1305855
Disease: Body mass index
Body mass index
1014 0 1 9.1E-04 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
681 0 1 1.3E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 1144 1 1.4E-03 1 8.5E-04
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.6E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 1 1.9E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.0E-03 0 0
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
399 0 1 2.1E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 2 2.2E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 2 2.3E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 2 2.3E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
338 0 1 2.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.5E-03 0 0
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
717 0 2 2.5E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 5 2.5E-03 0 0
CUI: C0541764
Disease: Delayed bone age
Delayed bone age
295 0 1 2.6E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.7E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 2 2.7E-03 0 0
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
283 0 1 2.7E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.8E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 2.9E-03 0 0
Red cell distribution width determination
593 0 2 3.0E-03 0 0
RDW - Red blood cell distribution width result
593 0 2 3.0E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 2 3.0E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.0E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 1 3.1E-03 0 0