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: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.17
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 1.6E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 1.9E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 1.9E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.1E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 2.2E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 2.2E-03 0 0
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 2.3E-03 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 1 2.3E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.3E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.3E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		130 0 1 2.3E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.3E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 2.3E-03 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 1 2.3E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 2.3E-03 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis 		121 0 1 2.3E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		118 0 1 2.3E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 2.3E-03 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 1 2.3E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 2.4E-03 0 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		112 0 1 2.4E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 2.4E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 2.4E-03 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 1 2.4E-03 0 0