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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
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.
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