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: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 0 1 1.1E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 1 1.3E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 1 1.3E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 1 1.4E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 1 1.5E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 3 1.5E-03 0 0
CUI: C0033377
Disease: Ptosis
Ptosis
607 0 1 1.6E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.6E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 1 1.6E-03 0 0
Delayed speech and language development
560 0 1 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.7E-03 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate
497 0 1 1.9E-03 0 0
CUI: C0239234
Disease: Low set ears
Low set ears
489 0 1 1.9E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 1 1.9E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 2.1E-03 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
429 0 1 2.1E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.4E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 2 2.5E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 2 2.5E-03 0 0
CUI: C0848558
Disease: Hypospadias
Hypospadias
366 0 1 2.5E-03 0 0
CUI: C0349588
Disease: Short stature
Short stature
1127 0 3 2.6E-03 0 0
CUI: C0302142
Disease: Deformity
Deformity
350 0 1 2.6E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 1 2.7E-03 0 0