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: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 1.00 0 0
CUI: C1835093
Disease: Masticatory Muscles, Hypertrophy of
Masticatory Muscles, Hypertrophy of 		1 0 1 1.00 0 0
CUI: C1836448
Disease: Nemaline myopathy 1
Nemaline myopathy 1 		1 10 1 1.00 2 0.20
CUI: C2750414
Disease: CAP MYOPATHY, TPM3-RELATED (disorder)
CAP MYOPATHY, TPM3-RELATED (disorder) 		1 0 1 1.00 0 0
CUI: C0265979
Disease: Fibrous Hamartoma of Infancy
Fibrous Hamartoma of Infancy 		3 0 1 0.33 0 0
CUI: C0751656
Disease: Nemaline Myopathy, Autosomal Dominant
Nemaline Myopathy, Autosomal Dominant 		4 0 1 0.25 0 0
CUI: C4025571
Disease: Type 1 fibers relatively smaller than type 2 fibers
Type 1 fibers relatively smaller than type 2 fibers 		6 0 1 0.17 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 1 0.14 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 1 0.14 0 0
CUI: C4025008
Disease: Reduced systolic function
Reduced systolic function 		8 0 1 0.12 0 0
CUI: C1266134
Disease: Spindle cell rhabdomyosarcoma
Spindle cell rhabdomyosarcoma 		9 0 1 0.11 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy 		9 0 1 0.11 0 0
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 1 1.0E-01 0 0
CUI: C3274592
Disease: Lipofibromatosis
Lipofibromatosis 		11 0 1 9.1E-02 0 0
CUI: C1847766
Disease: Shoulder girdle muscle atrophy
Shoulder girdle muscle atrophy 		12 0 1 8.3E-02 0 0
CUI: C4025729
Disease: Neuromuscular dysphagia
Neuromuscular dysphagia 		12 0 1 8.3E-02 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 1 7.7E-02 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 1 7.7E-02 0 0
CUI: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content 		14 0 1 7.1E-02 0 0
CUI: C3495721
Disease: Spitzoid melanoma
Spitzoid melanoma 		14 0 1 7.1E-02 0 0
CUI: C4022583
Disease: Fatiguable weakness of proximal limb muscles
Fatiguable weakness of proximal limb muscles 		14 0 1 7.1E-02 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 1 7.1E-02 0 0
CUI: C1853171
Disease: Multiple prenatal fractures
Multiple prenatal fractures 		15 0 1 6.7E-02 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 1 6.7E-02 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 1 6.2E-02 0 0