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GTR Home > Conditions/Phenotypes > Mitochondrial DNA depletion syndrome, encephalomyopathic form


A group of mitochondrial DNA maintenance syndrome diseases with characteristics of predominantly neuromuscular manifestations with typically infantile onset of hypotonia, lactic acidosis, psychomotor delay, progressive hyperkinetic-dystonic movement disorders, external ophthalmoplegia, sensorineural hearing loss, seizures and variable renal tubular dysfunction. It may be associated with a broad range of other clinical features. [from SNOMEDCT_US]

Available tests

5 tests are in the database for this condition.

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Genes See tests for all associated and related genes

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