Source: ALL
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: C0575081
Disease: Gait abnormality
Gait abnormality 		312 0 299 0.96 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 114 0.17 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 163 0.16 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0 		108 0 56 0.16 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0 		109 0 56 0.16 0 0
CUI: C0040822
Disease: Tremor
Tremor 		528 0 108 0.15 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 59 0.15 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 66 0.15 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 0 150 0.13 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		422 0 83 0.13 0 0
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia 		92 0 45 0.13 0 0
CUI: C2700617
Disease: Irritation - emotion
Irritation - emotion 		147 0 51 0.13 0 0
CUI: C4552810
Disease: Irritability, CTCAE
Irritability, CTCAE 		140 0 50 0.13 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood 		142 0 50 0.13 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		539 0 95 0.13 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 0 55 0.12 0 0
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome 		87 0 42 0.12 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 0 125 0.12 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		536 0 90 0.12 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 0 68 0.12 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		305 0 63 0.12 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 38 0.11 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		779 0 109 0.11 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		779 0 109 0.11 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 41 0.11 0 0