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Searched for "Mitochondrial Myopathies".

8 results found on Genetics Home Reference.

  1. mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes condition summary
    Related classification: Mitochondrial Myopathies
    Related genes and chromosomes:
  2. mitochondrial neurogastrointestinal encephalopathy disease condition summary
    Found in name or synonym: Mitochondrial myopathy with sensorimotor polyneuropathy,...
    Related genes:
  3. MT-TE gene summary
    Official name: mitochondrially encoded tRNA glutamic acid
    Found: ...involved in infantile transient mitochondrial myopathy (also known as benign COX deficiency...
  4. Kearns-Sayre syndrome condition summary
    Related classification: Mitochondrial Myopathies
    Related chromosomes:
  5. myoclonic epilepsy with ragged-red fibers condition summary
    Related classification: Mitochondrial Myopathies
    Related genes and chromosomes:
  6. progressive external ophthalmoplegia condition summary
    Related classification: Mitochondrial Myopathies
    Related genes and chromosomes:
  7. Can changes in mitochondrial DNA affect health and development? in the Handbook
    Found: ...part of their fact sheet called Mitochondrial Myopathies.
  8. PUS1 gene information
    Official name: pseudouridylate synthase 1
    Found: ...in this gene has been linked to mitochondrial myopathy and sideroblastic anemia. Alternate...
 
Published: May 20, 2013