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: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 11 12 9.3E-02 1 5.0E-02
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 5 9.3E-02 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia 		19 0 4 9.1E-02 0 0
CUI: C1855010
Disease: Progressive leukoencephalopathy
Progressive leukoencephalopathy 		7 0 3 9.1E-02 0 0
CUI: C4024705
Disease: Decreased activity of mitochondrial complex II
Decreased activity of mitochondrial complex II 		7 0 3 9.1E-02 0 0
CUI: C1533592
Disease: Malignant Paraganglionic Neoplasm
Malignant Paraganglionic Neoplasm 		8 0 3 8.8E-02 0 0
CUI: C1855578
Disease: Exercise-induced muscle cramps
Exercise-induced muscle cramps 		8 0 3 8.8E-02 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 9 8.7E-02 0 0
CUI: C1845245
Disease: Lower limb hypertonia
Lower limb hypertonia 		21 0 4 8.7E-02 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 7 8.6E-02 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 6 8.6E-02 0 0
CUI: C0345832
Disease: Neoplasm of small intestine
Neoplasm of small intestine 		9 0 3 8.6E-02 0 0
CUI: C0741933
Disease: cardiac symptom
cardiac symptom 		9 0 3 8.6E-02 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 3 9 8.6E-02 1 8.3E-02
CUI: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy 		9 0 3 8.6E-02 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 3 4 8.5E-02 1 8.3E-02
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 8 8.4E-02 0 0
CUI: C0410180
Disease: Eichsfeld type congenital muscular dystrophy
Eichsfeld type congenital muscular dystrophy 		10 0 3 8.3E-02 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		10 0 3 8.3E-02 0 0
CUI: C0751559
Disease: Pulsatile Tinnitus
Pulsatile Tinnitus 		23 0 4 8.3E-02 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 3 8.3E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 11 8.3E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 7 8.2E-02 0 0
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk 		37 0 5 8.2E-02 0 0
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia 		37 0 5 8.2E-02 0 0