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Mitochondrial DNA-related progressive external ophthalmoplegia

ORPHA:663

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
  • ICD-11: 9C82.0
  • OMIM: -
  • UMLS: C0162674
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

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 at the bottom of this page.

  A summary on this disease is available in Italiano (2004)

Detailed information

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Guidelines

Disease review articles

ERN produced/endorsed by ERN(s)   FSMR produced/endorsed by FSMR(s)

Additional information

Further information on this disease

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