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: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 0.50 0 0
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 0.50 0 0
CUI: C3888153
Disease: LONG QT SYNDROME 2, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 2, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 0.50 0 0
CUI: C4016248
Disease: LONG QT SYNDROME, BRADYCARDIA-INDUCED
LONG QT SYNDROME, BRADYCARDIA-INDUCED 		1 0 1 0.50 0 0
CUI: C4016724
Disease: RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE
RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE 		1 0 1 0.50 0 0
CUI: C4749335
Disease: Rippling muscle disease with myasthenia gravis
Rippling muscle disease with myasthenia gravis 		1 0 1 0.50 0 0
CUI: C4751434
Disease: Isolated asymptomatic elevation of creatine phosphokinase
Isolated asymptomatic elevation of creatine phosphokinase 		1 0 1 0.50 0 0
CUI: C0262918
Disease: Extraocular Muscle Paresis
Extraocular Muscle Paresis 		2 0 1 0.33 0 0
CUI: C1832560
Disease: RIPPLING MUSCLE DISEASE 2 (disorder)
RIPPLING MUSCLE DISEASE 2 (disorder) 		2 0 1 0.33 0 0
CUI: C1838254
Disease: RIPPLING MUSCLE DISEASE 1
RIPPLING MUSCLE DISEASE 1 		2 0 1 0.33 0 0
CUI: C2931401
Disease: Long QT syndrome type 3
Long QT syndrome type 3 		2 0 1 0.33 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC 		2 0 1 0.33 0 0
CUI: C3277700
Disease: LONG QT SYNDROME 1/2, DIGENIC (disorder)
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		2 0 1 0.33 0 0
CUI: C3280443
Disease: MYOPATHY, DISTAL, TATEYAMA TYPE
MYOPATHY, DISTAL, TATEYAMA TYPE 		2 0 1 0.33 0 0
CUI: C3805450
Disease: Calf muscle hypoplasia
Calf muscle hypoplasia 		2 0 1 0.33 0 0
CUI: C4022653
Disease: Abnormal muscle fiber protein expression
Abnormal muscle fiber protein expression 		2 0 1 0.33 0 0
CUI: C4280804
Disease: Percussion-induced rapid rolling muscle contractions
Percussion-induced rapid rolling muscle contractions 		2 0 1 0.33 0 0
CUI: C4724975
Disease: HyperCKmia
HyperCKmia 		2 0 1 0.33 0 0
CUI: C1853702
Disease: Muscle mounding
Muscle mounding 		3 0 1 0.25 0 0
CUI: C1865018
Disease: Short QT Syndrome 3
Short QT Syndrome 3 		3 0 1 0.25 0 0
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		3 0 1 0.25 0 0
CUI: C2931337
Disease: Chromosome 3, monosomy 3p25
Chromosome 3, monosomy 3p25 		3 0 1 0.25 0 0
CUI: C4053736
Disease: Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 		3 0 1 0.25 0 0
CUI: C0340464
Disease: Premature Cardiac Complex
Premature Cardiac Complex 		4 0 1 0.20 0 0
CUI: C1855579
Disease: Exercise-induced muscle stiffness
Exercise-induced muscle stiffness 		4 0 1 0.20 0 0