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: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance
0 1 0 0 1 3.5E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 2 6.9E-03
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 3.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.4E-03
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 4.7E-04 0 0
Shortening of all distal phalanges of the fingers
40 0 1 4.7E-04 0 0
CUI: C0018810
Disease: heart rate
heart rate
36 0 1 4.7E-04 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
35 0 1 4.7E-04 0 0
CUI: C0598275
Disease: Diffuse cerebral atrophy
Diffuse cerebral atrophy
34 0 1 4.7E-04 0 0
Moderate sensorineural hearing impairment
34 0 1 4.7E-04 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 1 4.7E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia
33 0 1 4.7E-04 0 0
CUI: C4021620
Disease: Clinodactyly of the 2nd toe
Clinodactyly of the 2nd toe
32 0 1 4.7E-04 0 0
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
30 0 1 4.7E-04 0 0
CUI: C1843637
Disease: Neck flexor weakness
Neck flexor weakness
30 0 1 4.7E-04 0 0
CUI: C4021757
Disease: EEG with polyspike wave complexes
EEG with polyspike wave complexes
30 0 1 4.7E-04 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination
29 0 1 4.7E-04 0 0
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block
26 0 1 4.7E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
26 0 1 4.7E-04 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position
26 0 1 4.7E-04 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc
26 0 1 4.7E-04 0 0
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe
26 0 1 4.7E-04 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change
24 0 1 4.7E-04 0 0
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
24 0 1 4.7E-04 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding)
23 0 1 4.7E-04 0 0