Disease: Mitochondrial Encephalomyopathies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		0.300 Biomarker disease CTD_human Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect. 20598281 2010