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: C1855579
Disease: Exercise-induced muscle stiffness
Exercise-induced muscle stiffness 		4 1 3 0.33 1 1.00
CUI: C0027080
Disease: Myoglobinuria
Myoglobinuria 		17 0 4 0.19 0 0
CUI: C0268634
Disease: Disorder of fatty acid metabolism
Disorder of fatty acid metabolism 		6 0 2 0.17 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis 		6 1 2 0.17 1 1.00
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism 		7 0 2 0.15 0 0
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		8 0 2 0.14 0 0
CUI: C0017926
Disease: Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VII 		9 0 2 0.13 0 0
CUI: C0270984
Disease: Metabolic myopathy
Metabolic myopathy 		18 0 3 0.13 0 0
CUI: C1855580
Disease: Exercise-induced muscle fatigue
Exercise-induced muscle fatigue 		18 3 3 0.13 1 0.33
CUI: C0155145
Disease: Chronic conjunctivitis
Chronic conjunctivitis 		1 0 1 0.12 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 0.12 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.12 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.12 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 0.12 0 0
CUI: C1689817
Disease: Cardiomyopathy associated with another disorder
Cardiomyopathy associated with another disorder 		10 0 2 0.12 0 0
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia 		37 4 5 0.12 1 0.25
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 0.12 0 0
CUI: C1855577
Disease: Erythrocyte Lactate Transporter Defect
Erythrocyte Lactate Transporter Defect 		1 0 1 0.12 0 0
CUI: C1864902
Disease: Hyperinsulinemic hypoglycemia, familial, 7
Hyperinsulinemic hypoglycemia, familial, 7 		1 0 1 0.12 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 0.12 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 0.12 0 0
CUI: C4015186
Disease: MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY 		1 0 1 0.12 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 0.12 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 0.12 0 0
CUI: C4016683
Disease: MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL RECESSIVE
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL RECESSIVE 		1 0 1 0.12 0 0