Disease: Myalgia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0231528
Disease: Myalgia
Myalgia 		0.110 GeneticVariation phenotype BEFREE A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence. 22000755 2011
CUI: C0231528
Disease: Myalgia
Myalgia 		0.110 Biomarker phenotype HPO