TRNW, tRNA, 4578

N. diseases: 188; N. variants: 7
Disease: Mitochondrial Myopathies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.410 GeneticVariation group BEFREE A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy. 23841600 2014
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.410 CausalMutation group CLINVAR
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.410 Biomarker group CTD_human
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.410 Biomarker group HPO