C0022541_NCI_NICHD | Knowledge4COVID-19

Property	Value
?:definition	A genetically heterogenous condition caused by various deletions of mitochondrial DNA. The condition is characterized by myopathy, with \'ragged red\' fibers on histopathology of muscle biopsy, progressive external ophthalmoplegia, pigmentary retinopathy, cardiac conduction defects, ataxia, cognitive impairment, and diabetes mellitus.
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