Source: INFERRED ×
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 32 0.15 31 9.3E-02
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		22 27 13 0.13 15 0.12
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 58 14 0.11 15 9.3E-02
CUI: C0014877
Disease: Esotropia
Esotropia 		121 39 21 0.11 12 8.3E-02
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		41 56 12 0.10 12 7.4E-02
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 11 1.0E-01 11 7.6E-02
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 411 27 9.9E-02 14 2.7E-02
CUI: C1854882
Disease: Absent speech
Absent speech 		232 72 28 9.6E-02 16 9.2E-02
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		459 62 45 8.9E-02 12 7.1E-02
CUI: C0015310
Disease: Exotropia
Exotropia 		72 21 13 8.8E-02 7 5.3E-02
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		335 611 34 8.7E-02 8 1.1E-02
CUI: C1837142
Disease: Poor suck
Poor suck 		103 31 14 7.9E-02 14 0.10
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 23 19 7.7E-02 6 4.4E-02
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		192 41 20 7.7E-02 9 6.0E-02
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 6 14 7.5E-02 1 8.1E-03
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure 		91 16 12 7.1E-02 5 3.9E-02
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 19 12 7.1E-02 9 7.0E-02
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 54 17 7.0E-02 10 6.2E-02
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis 		66 24 10 6.9E-02 7 5.2E-02
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		237 350 21 6.9E-02 6 1.3E-02
CUI: C0239234
Disease: Low set ears
Low set ears 		489 64 37 6.8E-02 7 4.0E-02
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 50 14 6.8E-02 12 7.7E-02
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		210 32 19 6.8E-02 2 1.4E-02
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		116 59 13 6.8E-02 5 2.9E-02
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 24 13 6.7E-02 7 5.2E-02