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: C3807025
Disease: Intermittent episodes of respiratory insufficiency due to muscle weakness
Intermittent episodes of respiratory insufficiency due to muscle weakness 		14 0 11 0.14 0 0
CUI: C4025671
Disease: Sudden episodic apnea
Sudden episodic apnea 		14 0 11 0.14 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 15 0.14 0 0
CUI: C0751883
Disease: Congenital Myasthenic Syndromes, Postsynaptic
Congenital Myasthenic Syndromes, Postsynaptic 		18 0 11 0.13 0 0
CUI: C0751885
Disease: Myasthenic Syndromes, Congenital, Slow Channel
Myasthenic Syndromes, Congenital, Slow Channel 		18 0 11 0.13 0 0
CUI: C1859438
Disease: Frontalis muscle weakness
Frontalis muscle weakness 		10 0 10 0.13 0 0
CUI: C4021066
Disease: Narrow jaw
Narrow jaw 		11 0 10 0.13 0 0
CUI: C4022168
Disease: EMG: impaired neuromuscular transmission
EMG: impaired neuromuscular transmission 		11 0 10 0.13 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 11 0.13 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 12 0.13 0 0
CUI: C0162297
Disease: Respiratory arrest
Respiratory arrest 		12 0 10 0.13 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 10 0.13 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 10 0.13 0 0
CUI: C1843637
Disease: Neck flexor weakness
Neck flexor weakness 		30 0 12 0.13 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 0 14 0.13 0 0
CUI: C0038450
Disease: Stridor
Stridor 		31 0 12 0.13 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 0 15 0.12 0 0
CUI: C3809827
Disease: Staring gaze
Staring gaze 		16 0 10 0.12 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 13 0.12 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 14 0.12 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 24 14 0.12 1 3.6E-02
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 16 22 0.12 3 0.17
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 12 0.12 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 20 0.12 0 0
CUI: C2830004
Disease: Somnolence
Somnolence 		87 0 17 0.12 0 0