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: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE
299 0 299 0.96 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 54 119 0.17 1 1.3E-02
CUI: C0004134
Disease: Ataxia
Ataxia
868 68 166 0.16 1 1.1E-02
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 57 0.16 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 57 0.16 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
213 0 69 0.15 0 0
CUI: C0040822
Disease: Tremor
Tremor
528 0 110 0.15 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign
155 0 59 0.14 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 579 154 0.14 5 8.4E-03
CUI: C3665347
Disease: Visual Impairment
Visual Impairment
422 0 85 0.13 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 19 98 0.13 1 2.4E-02
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia
92 0 46 0.13 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 135 132 0.13 2 1.3E-02
CUI: C2700617
Disease: Irritation - emotion
Irritation - emotion
147 0 52 0.13 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 87 96 0.13 3 2.8E-02
CUI: C4552810
Disease: Irritability, CTCAE
Irritability, CTCAE
140 0 51 0.13 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood
142 0 51 0.13 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 80 71 0.12 1 9.8E-03
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 56 0.12 0 0
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome
87 0 43 0.12 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 64 0.12 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 112 0.11 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 112 0.11 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 93 0.11 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
306 0 63 0.11 0 0