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: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
393 0 1 2.0E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.1E-03 0 0
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
300 0 1 2.5E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
265 0 1 2.8E-03 0 0
CUI: C4317109
Disease: Epileptic Seizures
Epileptic Seizures
250 0 1 2.9E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 2.9E-03 0 0
Creatine phosphokinase serum increased
228 0 1 3.1E-03 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
228 0 1 3.1E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 3.1E-03 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
226 0 1 3.1E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 1 3.1E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 3.1E-03 0 0
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
218 0 1 3.2E-03 0 0
CUI: C0030552
Disease: Paresis
Paresis
216 0 1 3.2E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
210 0 1 3.3E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 3.3E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 3.3E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 3.4E-03 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration
195 0 1 3.4E-03 0 0
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome
194 0 1 3.5E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 1 3.5E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 3.5E-03 0 0
CUI: C0033375
Disease: Prolactinoma
Prolactinoma
187 0 1 3.5E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 3.5E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 1 3.6E-03 0 0