Disease: Myopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026848
Disease: Myopathy
Myopathy 		0.300 Biomarker group CTD_human Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia. 22961002 2012