OBO ID: DOID:0112065 |
Term Name: | nuclear type mitochondrial complex I deficiency | Search Ontology: | |
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Synonyms: |
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Definition: | A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome. (2) | ||
References: | |||
Ontology: | Human Disease ( DOID:0112065 ) |
OTHER nuclear type mitochondrial complex I deficiency PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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