OBO ID: DOID:0080112 |
Term Name: | mitochondrial complex III deficiency nuclear type 3 | Search Ontology: | |
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Definition: | A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRB gene on chromosome 8q22. http://omim.org/entry/615158?search=615158&highlight=615158 | ||
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Ontology: | Human Disease ( DOID:0080112 ) |
OTHER mitochondrial complex III deficiency nuclear type 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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