OBO ID: DOID:0111491 |
Term Name: | combined oxidative phosphorylation deficiency 15 | Search Ontology: | |
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Definition: | A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation] in the MTFMT gene on chromosome 15q22.31. https://www.ncbi.nlm.nih.gov/pubmed/21907147 | ||
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Ontology: | Human Disease ( DOID:0111491 ) |
OTHER combined oxidative phosphorylation deficiency 15 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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