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: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 1 1.0E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 2 1.0E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 1 1.2E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 1 1.2E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 1 1.3E-03 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
681 0 1 1.4E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.5E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 2 1.5E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 1 1.6E-03 0 0
Red cell distribution width determination
593 0 1 1.6E-03 0 0
RDW - Red blood cell distribution width result
593 0 1 1.6E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 1 1.6E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 1 1.6E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.7E-03 0 0
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
565 0 1 1.7E-03 0 0
CUI: C0349588
Disease: Short stature
Short stature
1127 0 2 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.7E-03 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 1 1.8E-03 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 1 1.9E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-03 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE
1010 0 2 1.9E-03 0 0
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
486 0 1 1.9E-03 0 0
Low density lipoprotein cholesterol measurement
483 0 1 1.9E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 2.0E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 0 1 2.2E-03 0 0