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: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis
112 0 38 0.14 0 0
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE
299 0 55 0.12 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
312 0 56 0.12 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 33 0.12 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 33 0.12 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 27 43 0.11 1 2.1E-02
CUI: C0018524
Disease: Hallucinations
Hallucinations
178 0 38 0.11 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
43 0 24 0.11 0 0
CUI: C2700617
Disease: Irritation - emotion
Irritation - emotion
147 0 34 0.11 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 13 46 0.11 1 3.0E-02
CUI: C4552810
Disease: Irritability, CTCAE
Irritability, CTCAE
140 0 33 0.11 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood
142 0 33 0.11 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 34 44 0.11 1 1.9E-02
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 80 50 0.10 2 2.0E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 579 108 0.10 2 3.3E-03
Aplasia/Hypoplasia of the cerebellum
116 0 29 0.10 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
210 32 36 9.7E-02 3 6.0E-02
CUI: C1858430
Disease: Death in infancy
Death in infancy
146 0 30 9.6E-02 0 0
CUI: C0151526
Disease: Premature Birth
Premature Birth
192 50 34 9.6E-02 2 2.9E-02
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 22 42 9.1E-02 1 2.4E-02
CUI: C0152421
Disease: Macrotia
Macrotia
188 18 32 9.1E-02 1 2.6E-02
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 164 95 9.0E-02 3 1.6E-02
CUI: C0038379
Disease: Strabismus
Strabismus
716 89 73 8.7E-02 2 1.9E-02
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 26 8.7E-02 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign
155 0 28 8.6E-02 0 0