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| Term | mitochondrial complex III deficiency nuclear type 4 | ID (Ontology) | DOID:0080113 (Human Disease) |
| Definition | A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRQ gene on chromosome 5q31. | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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mitochondrial metabolism disease |__mitochondrial complex III deficiency |__mitochondrial complex III deficiency nuclear type 4 1 rec. |
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| Is a | mitochondrial complex III deficiency | ||
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| MIM:615159 | |||