Mitochondrial Encephalomyopathy

About the Disease
Mitochondrial Encephalomyopathy, also known as mitochondrial encephalomyopathies, is related to mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes and combined oxidative phosphorylation deficiency 6. An important gene associated with Mitochondrial Encephalomyopathy is MT-CYB (Mitochondrially Encoded Cytochrome B), and among its related pathways/superpathways are Metabolism and "Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.". The drugs 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, brain and occipital lobe.

Common Targets
TMEM70 | NSUN3 | SLC25A42 | DNM1L | SLIRP | ATP6 | ATP8 | COX11 | LIG3 | FASTKD2 | TYMP | MRPS25

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