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| Term | nuclear type mitochondrial complex I deficiency | ID (Ontology) | DOID:0112065 (Human Disease) | |||||
| Definition | A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome. | |||||||
| Also Known As | "MC1DN" | |||||||
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| Is a | mitochondrial complex I deficiency | ||
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External Crossreferences & Linkouts
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| MIM:PS252010 | |||