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: C0026010
Disease: Microphthalmos
Microphthalmos
337 0 88 0.13 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
312 0 85 0.13 0 0
CUI: C0040822
Disease: Tremor
Tremor
528 0 110 0.13 0 0
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE
299 0 83 0.13 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 66 0.13 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 95 0.13 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 81 0.13 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 164 0.12 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
285 0 78 0.12 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
590 0 110 0.12 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 109 0.12 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE
1010 0 154 0.12 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 0 104 0.12 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 81 0.12 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 90 0.12 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 96 0.12 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 0 74 0.12 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density
76 0 53 0.12 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
407 0 88 0.12 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 60 0.12 0 0
CUI: C0349588
Disease: Short stature
Short stature
1127 0 162 0.12 0 0
Aplasia/Hypoplasia of the cerebellum
116 0 56 0.12 0 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
1825 0 231 0.11 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 104 0.11 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 0 128 0.11 0 0