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: C0268958
Disease: Acute orchitis
Acute orchitis
0 1 0 0 1 0.14
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania
0 1 0 0 1 0.14
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 0.14
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 6.7E-02
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain
0 2 0 0 1 0.12
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 0.11
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 0.11
CUI: C0037369
Disease: Smoking
Smoking
391 765 1 1.7E-03 1 1.3E-03
CUI: C0521525
Disease: Short neck
Short neck
288 0 1 2.0E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 2.1E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 742 1 2.2E-03 1 1.3E-03
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 2.3E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 2.3E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears
223 0 1 2.3E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 0 1 2.4E-03 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
210 0 1 2.4E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.4E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 2.4E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 2.5E-03 0 0
CUI: C3553764
Disease: Joint hyperflexibility
Joint hyperflexibility
181 0 1 2.6E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 2.7E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers
171 0 1 2.7E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
160 0 1 2.7E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
160 246 1 2.7E-03 1 4.0E-03
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.8E-03 0 0