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: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
160 246 10 3.9E-02 1 2.7E-03
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding
82 0 7 3.9E-02 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 24 3.9E-02 0 0
CUI: C1849172
Disease: Frontal lobe hypoplasia
Frontal lobe hypoplasia
30 0 5 3.9E-02 0 0
CUI: C0239234
Disease: Low set ears
Low set ears
489 0 22 3.9E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea
31 0 5 3.8E-02 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 15 3.8E-02 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 10 3.8E-02 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 16 3.8E-02 0 0
CUI: C1261470
Disease: Congenital meningocele
Congenital meningocele
33 0 5 3.8E-02 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 14 3.8E-02 0 0
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
535 0 23 3.7E-02 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly
148 0 9 3.7E-02 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 13 3.7E-02 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 9 3.7E-02 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly
37 0 5 3.7E-02 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases
66 0 6 3.7E-02 0 0
Malformations of Cortical Development, Group II
180 0 10 3.6E-02 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor
95 0 7 3.6E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 7 3.6E-02 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment
67 0 6 3.6E-02 0 0
CUI: C1836047
Disease: Long face
Long face
182 0 10 3.6E-02 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 0 10 3.6E-02 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders
183 0 10 3.6E-02 0 0
CUI: C1855675
Disease: Arima syndrome
Arima syndrome
11 0 4 3.6E-02 0 0