Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
0.100 CausalMutation phenotype CLINVAR Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model. 20883824 2011
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
0.100 CausalMutation phenotype CLINVAR A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. 20142534 2010
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
0.100 Biomarker phenotype HPO