Disease: Neurogenic Muscular Atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270948
Disease: Neurogenic Muscular Atrophy
Neurogenic Muscular Atrophy 		0.300 Biomarker phenotype CTD_human Merg1a K+ channel induces skeletal muscle atrophy by activating the ubiquitin proteasome pathway. 16723379 2006