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: C0521732
Disease: Lower eyelid entropion
Lower eyelid entropion 		2 0 2 0.67 0 0
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		2 0 2 0.67 0 0
CUI: C0152226
Disease: Lagophthalmos
Lagophthalmos 		3 0 2 0.50 0 0
CUI: C0155188
Disease: Senile entropion
Senile entropion 		3 0 2 0.50 0 0
CUI: C1959600
Disease: Obscure African cardiomyopathy
Obscure African cardiomyopathy 		1 0 1 0.33 0 0
CUI: C4025575
Disease: Myotonia with warm-up phenomenon
Myotonia with warm-up phenomenon 		1 0 1 0.33 0 0
CUI: C4025883
Disease: Abnormality of lower lip
Abnormality of lower lip 		1 0 1 0.33 0 0
CUI: C4304532
Disease: 2q23.1 microdeletion syndrome
2q23.1 microdeletion syndrome 		1 0 1 0.33 0 0
CUI: C0270959
Disease: Myotonia Levior
Myotonia Levior 		2 0 1 0.25 0 0
CUI: C0751360
Disease: Becker Generalized Myotonia
Becker Generalized Myotonia 		2 0 1 0.25 0 0
CUI: C2931139
Disease: Nondystrophic myotonia
Nondystrophic myotonia 		2 0 1 0.25 0 0
CUI: C4022683
Disease: Myotonia of the upper limb
Myotonia of the upper limb 		2 0 1 0.25 0 0
CUI: C1828221
Disease: Non dystrophic myotonia
Non dystrophic myotonia 		3 0 1 0.20 0 0
CUI: C1850663
Disease: Muscle hypertrophy of the lower extremities
Muscle hypertrophy of the lower extremities 		3 0 1 0.20 0 0
CUI: C4025576
Disease: EMG: myotonic runs
EMG: myotonic runs 		3 0 1 0.20 0 0
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis 		4 0 1 0.17 0 0
CUI: C1839749
Disease: Paroxysmal bursts of laughter
Paroxysmal bursts of laughter 		4 0 1 0.17 0 0
CUI: C1868623
Disease: Handgrip myotonia
Handgrip myotonia 		4 0 1 0.17 0 0
CUI: C4022169
Disease: EMG: myotonic discharges
EMG: myotonic discharges 		4 0 1 0.17 0 0
CUI: C0751359
Disease: Percussion Myotonia
Percussion Myotonia 		5 0 1 0.14 0 0
CUI: C0751340
Disease: Myasthenia Gravis, Ocular
Myasthenia Gravis, Ocular 		17 0 2 0.11 0 0
CUI: C0027127
Disease: Myotonia Congenita
Myotonia Congenita 		9 0 1 9.1E-02 0 0
CUI: C0154676
Disease: Organic writer's cramp
Organic writer's cramp 		9 0 1 9.1E-02 0 0
CUI: C0553604
Disease: Myotonic Disorders
Myotonic Disorders 		9 0 1 9.1E-02 0 0
CUI: C1869117
Disease: Paroxysmal nonkinesigenic dyskinesia
Paroxysmal nonkinesigenic dyskinesia 		10 0 1 8.3E-02 0 0