OBO ID: DOID:3762 |
Term Name: | cytochrome-c oxidase deficiency disease | Search Ontology: | |
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Definition: | A mitochondrial metabolism disease that is characterized by deficiency of cytochrome c oxidase, myopathy, hepatomegaly, hypertrophic cardiomyopathy, lactic acidosis, and Leigh syndrome, and is caused by mutations related to oxidative phosphorylation. (3) | ||
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Ontology: | Human Disease ( DOID:3762 ) |
OTHER cytochrome-c oxidase deficiency disease PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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