Orphanet: Mitochondrial oxidative phosphorylation disorder due to a large scale single deletion of mitochondrial DNA
x

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA

ORPHA:254767

Classification level: Group of disorders
  • Synonym(s):
    • Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mtDNA
    • OXPHOS disease due to a large-scale single deletion of mitochondrial DNA
    • OXPHOS disease due to a large-scale single deletion of mtDNA
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: -
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Additional information

Further information on this disease

Health care resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.