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: C0027127
Disease: Myotonia Congenita
Myotonia Congenita 		9 38 8 0.47 27 0.38
CUI: C0751359
Disease: Percussion Myotonia
Percussion Myotonia 		5 0 3 0.17 0 0
CUI: C0553604
Disease: Myotonic Disorders
Myotonic Disorders 		9 0 3 0.14 0 0
CUI: C1869117
Disease: Paroxysmal nonkinesigenic dyskinesia
Paroxysmal nonkinesigenic dyskinesia 		10 0 3 0.13 0 0
CUI: C0027125
Disease: Myotonia
Myotonia 		19 7 4 0.13 3 4.6E-02
CUI: C0270959
Disease: Myotonia Levior
Myotonia Levior 		2 1 2 0.12 1 1.6E-02
CUI: C0751360
Disease: Becker Generalized Myotonia
Becker Generalized Myotonia 		2 67 2 0.12 45 0.54
CUI: C2931139
Disease: Nondystrophic myotonia
Nondystrophic myotonia 		2 0 2 0.12 0 0
CUI: C4022683
Disease: Myotonia of the upper limb
Myotonia of the upper limb 		2 2 2 0.12 1 1.6E-02
CUI: C0751358
Disease: Myotonic Phenomenon
Myotonic Phenomenon 		3 0 2 0.12 0 0
CUI: C1828221
Disease: Non dystrophic myotonia
Non dystrophic myotonia 		3 0 2 0.12 0 0
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis 		4 0 2 0.11 0 0
CUI: C1868623
Disease: Handgrip myotonia
Handgrip myotonia 		4 0 2 0.11 0 0
CUI: C4022169
Disease: EMG: myotonic discharges
EMG: myotonic discharges 		4 3 2 0.11 1 1.6E-02
CUI: C1851936
Disease: Paroxysmal choreoathetosis
Paroxysmal choreoathetosis 		5 0 2 0.11 0 0
CUI: C0037997
Disease: Splenic Diseases
Splenic Diseases 		6 0 2 1.0E-01 0 0
CUI: C1842534
Disease: DYSTONIA 18 (disorder)
DYSTONIA 18 (disorder) 		6 0 2 1.0E-01 0 0
CUI: C0238358
Disease: Hypokalemic periodic paralysis
Hypokalemic periodic paralysis 		19 0 3 9.4E-02 0 0
CUI: C2265792
Disease: Skeletal muscle hypertrophy
Skeletal muscle hypertrophy 		21 0 3 8.8E-02 0 0
CUI: C0154676
Disease: Organic writer's cramp
Organic writer's cramp 		9 0 2 8.7E-02 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 2 8.3E-02 0 0
CUI: C4316810
Disease: Writer's Cramp
Writer's Cramp 		26 0 3 7.7E-02 0 0
CUI: C0520571
Disease: Fibrosis of bile duct
Fibrosis of bile duct 		13 0 2 7.4E-02 0 0
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		13 0 2 7.4E-02 0 0
CUI: C3469605
Disease: PSEUDOHYPOALDOSTERONISM, TYPE IID
PSEUDOHYPOALDOSTERONISM, TYPE IID 		13 0 2 7.4E-02 0 0