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Mitochondrial DNA-related progressive external ophthalmoplegia

Disease definition

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.


Classification level: Disorder
  • Synonym(s):
    • Maternally-inherited CPEO
    • Maternally-inherited chronic progressive external ophthalmoplegia
    • mtDNA-related progressive external ophthalmoplegia
  • Prevalence: Unknown
  • Inheritance: Mitochondrial inheritance or Not applicable 
  • Age of onset: Adolescent, Adult
  • ICD-10: H49.4
  • OMIM: -
  • UMLS: C0162674
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

Article for general public


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