Disease: Myopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026848
Disease: Myopathy
Myopathy 		0.010 GeneticVariation group BEFREE Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2. 20405137 2010