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: C0543859
Disease: Amyotrophic Lateral Sclerosis, Guam Form
Amyotrophic Lateral Sclerosis, Guam Form 		36 0 29 0.78 0 0
CUI: C4022588
Disease: Fatigable weakness of swallowing muscles
Fatigable weakness of swallowing muscles 		39 0 13 0.23 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 8 0.23 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 13 0.20 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 13 0.18 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 13 0.17 0 0
CUI: C0522224
Disease: Paralysed
Paralysed 		68 0 13 0.15 0 0
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 7 0.15 0 0
CUI: C1849485
Disease: Neuronal loss in the cerebral cortex
Neuronal loss in the cerebral cortex 		8 0 5 0.15 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 6 0.14 0 0
CUI: C4025723
Disease: Abnormal upper motor neuron morphology
Abnormal upper motor neuron morphology 		20 0 6 0.14 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 6 0.13 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 6 0.13 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 5 0.13 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 6 0.13 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 13 0.12 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 13 0.12 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 7 0.12 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis 		19 0 5 0.11 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy 		19 0 5 0.11 0 0
CUI: C3714618
Disease: Primary Hyperthyroidism
Primary Hyperthyroidism 		10 0 4 0.11 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies 		44 0 7 0.10 0 0
CUI: C0085631
Disease: Agitation
Agitation 		109 0 13 0.10 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 13 9.7E-02 0 0
CUI: C0205875
Disease: Papillomatosis
Papillomatosis 		18 0 4 9.1E-02 0 0