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: C0005890
Disease: Body Height
Body Height
1903 0 3 1.5E-03 0 0
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
565 0 1 1.6E-03 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate
497 0 1 1.8E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 1.9E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 1 2.0E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.1E-03 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation
340 0 1 2.5E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
338 0 1 2.5E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 2 2.6E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.6E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 2 2.8E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.8E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck
288 0 1 2.8E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 0 1 2.9E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 3.0E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 0 1 3.0E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 3.0E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose
265 0 1 3.0E-03 0 0
Red cell distribution width determination
593 0 2 3.1E-03 0 0
RDW - Red blood cell distribution width result
593 0 2 3.1E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 3.1E-03 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
590 0 2 3.1E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 2 3.1E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.1E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 3.2E-03 0 0