Orphanet: Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

Search for a rare disease

Other search option(s)

Alphabetical list

Suggest an update

(*) Required fields.

You are (*)

If you have selected the “Other” category, please specify which type of user you are: *

Email address: *

Topic of your comment *

Epidemiology data

Clinical signs

Nomenclature and/or coding

Your message *

(3000 characters remaining)

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.

Check this box if you wish to receive a copy of your message

Please reproduce the text below: *

Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

ORPHA:254776

Classification level: Group of disorders

Synonym(s):
- Mitochondrial oxidative phosphorylation disorder due to a point mutation of mtDNA
- OXPHOS disease due to a point mutation of mitochondrial DNA
- OXPHOS disease due to a point mutation 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.

Detailed information

Professionals

Clinical genetics review
English (2014)

Additional information

Further information on this disease

Health care resources for this disease

Research activities on this disease

Specialised Social Services

Eurordis directory

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.