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: C0009398
Disease: Color vision defect
Color vision defect
0 4 0 0 2 0.12
CUI: C0394006
Disease: Dysequilibrium syndrome
Dysequilibrium syndrome
0 1 0 0 1 7.1E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 4.5E-02
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder)
0 1 0 0 1 7.1E-02
CUI: C0349588
Disease: Short stature
Short stature
1127 0 1 8.6E-04 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE
1010 0 1 9.5E-04 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 1 1.0E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 1 1.3E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 1 1.5E-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: 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: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 2 2.0E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 4 2.1E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.1E-03 0 0
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
439 0 1 2.1E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 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: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
426 0 1 2.1E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 2 2.3E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 2 2.3E-03 0 0