Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
colon (non-specific) polyp hyperplastic
1 0 1 0.50 0 0
Neuropathy, Distal Hereditary Motor, Type VIIA
1 0 1 0.50 0 0
MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC
1 0 1 0.50 0 0
CUI: C1834015
Disease: Progressive ptosis
Progressive ptosis
2 0 1 0.33 0 0
Generalized hypotonia due to defect at the neuromuscular junction
2 0 1 0.33 0 0
MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC
2 0 1 0.33 0 0
Distal hereditary motor neuropathy type 7
2 0 1 0.33 0 0
Familial Olivopontocerebellar Atrophy
3 0 1 0.25 0 0
Vaccine associated paralytic poliomyelitis
3 0 1 0.25 0 0
CUI: C1859438
Disease: Frontalis muscle weakness
Frontalis muscle weakness
10 0 2 0.20 0 0
CUI: C4021066
Disease: Narrow jaw
Narrow jaw
11 0 2 0.18 0 0
EMG: impaired neuromuscular transmission
11 0 2 0.18 0 0
CUI: C0162297
Disease: Respiratory arrest
Respiratory arrest
12 0 2 0.17 0 0
CUI: C1963788
Disease: Peripheral nerve lesion
Peripheral nerve lesion
5 0 1 0.17 0 0
Apneic episodes precipitated by illness, fatigue, stress
12 0 2 0.17 0 0
CUI: C4280747
Disease: Choking episodes
Choking episodes
12 0 2 0.17 0 0
CUI: C0232608
Disease: Nasal regurgitation
Nasal regurgitation
14 0 2 0.14 0 0
Intermittent episodes of respiratory insufficiency due to muscle weakness
14 0 2 0.14 0 0
CUI: C4025671
Disease: Sudden episodic apnea
Sudden episodic apnea
14 0 2 0.14 0 0
CUI: C3809827
Disease: Staring gaze
Staring gaze
16 0 2 0.12 0 0
CUI: C4255193
Disease: Bilateral Vestibulopathy
Bilateral Vestibulopathy
7 0 1 0.12 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress
21 0 2 9.5E-02 0 0
Partial Paralysis (Paresis) Vocal Cords
10 0 1 9.1E-02 0 0
CUI: C0333751
Disease: Muscle fiber atrophy
Muscle fiber atrophy
25 0 2 8.0E-02 0 0
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome
12 0 1 7.7E-02 0 0