TRNE, tRNA, 4556

N. diseases: 83; N. variants: 4
Disease: MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3151898
Disease: MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT
MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT 		0.400 CausalMutation disease CLINVAR
CUI: C3151898
Disease: MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT
MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT 		0.400 GermlineCausalMutation disease ORPHANET Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. 19720722 2009