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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
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.
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