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: C4073190
Disease: Abnormality of masticatory muscle
Abnormality of masticatory muscle 		17 0 12 0.18 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 57 0.18 0 0
CUI: C2230441
Disease: Triceps weakness
Triceps weakness 		18 0 12 0.18 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 15 0.18 0 0
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure 		319 0 56 0.17 0 0
CUI: C0393554
Disease: Amyotrophic Lateral Sclerosis With Dementia
Amyotrophic Lateral Sclerosis With Dementia 		30 0 13 0.17 0 0
CUI: C4021728
Disease: EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation 		24 0 12 0.17 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		222 0 40 0.17 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 10 0.16 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 11 0.16 0 0
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 11 0.15 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 12 0.15 0 0
CUI: C0543859
Disease: Amyotrophic Lateral Sclerosis, Guam Form
Amyotrophic Lateral Sclerosis, Guam Form 		36 0 12 0.14 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 10 0.14 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		61 0 15 0.14 0 0
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting 		257 0 37 0.13 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 20 0.13 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis 		54 0 13 0.13 0 0
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		99 0 18 0.13 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 9 0.12 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 13 0.12 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 16 0.12 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 12 0.12 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 11 0.12 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 9 0.12 0 0