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: C0856123
Disease: Myotonia aggravated
Myotonia aggravated
1 0 1 1.00 0 0
PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
1 0 1 1.00 0 0
Normokalemic Periodic Paralysis, Potassium-Sensitive
1 0 1 1.00 0 0
Paramyotonia Congenita Without Cold Paralysis
1 0 1 1.00 0 0
LARYNGOSPASM, SEVERE NEONATAL EPISODIC
1 0 1 1.00 0 0
CUI: C3280112
Disease: MYASTHENIC SYNDROME, CONGENITAL, 16
MYASTHENIC SYNDROME, CONGENITAL, 16
1 0 1 1.00 0 0
Hyperkalemic Periodic Paralysis Type 2
1 0 1 1.00 0 0
PARAMYOTONIA CONGENITA/MYOTONIA CONGENITA
1 0 1 1.00 0 0
MYOTONIA CONGENITA, ATYPICAL, ACETAZOLAMIDE-RESPONSIVE
1 0 1 1.00 0 0
CUI: C4022682
Disease: Cold-sensitive myotonia
Cold-sensitive myotonia
1 0 1 1.00 0 0
CUI: C4022684
Disease: Myotonia of the lower limb
Myotonia of the lower limb
1 0 1 1.00 0 0
CUI: C4022685
Disease: Myotonia of the jaw
Myotonia of the jaw
1 0 1 1.00 0 0
CUI: C4022686
Disease: Myotonia of the face
Myotonia of the face
1 0 1 1.00 0 0
CUI: C4022691
Disease: Facial muscle hypertrophy
Facial muscle hypertrophy
1 0 1 1.00 0 0
CUI: C4531172
Disease: Cold paresis
Cold paresis
1 0 1 1.00 0 0
CUI: C0268445
Disease: Normokalemic Periodic Paralysis
Normokalemic Periodic Paralysis
2 0 1 0.50 0 0
CUI: C0270959
Disease: Myotonia Levior
Myotonia Levior
2 0 1 0.50 0 0
CUI: C0751360
Disease: Becker Generalized Myotonia
Becker Generalized Myotonia
2 0 1 0.50 0 0
Hypokalemic Periodic Paralysis, Type 2
2 0 1 0.50 0 0
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
2 0 1 0.50 0 0
CUI: C2931139
Disease: Nondystrophic myotonia
Nondystrophic myotonia
2 0 1 0.50 0 0
CUI: C4021979
Disease: Muscular edema
Muscular edema
2 0 1 0.50 0 0
CUI: C4022683
Disease: Myotonia of the upper limb
Myotonia of the upper limb
2 0 1 0.50 0 0
CUI: C4025281
Disease: Neonatal inspiratory stridor
Neonatal inspiratory stridor
2 0 1 0.50 0 0
CUI: C0751358
Disease: Myotonic Phenomenon
Myotonic Phenomenon
3 0 1 0.33 0 0