OBO ID: DOID:0112093 |
Term Name: | nuclear type mitochondrial complex I deficiency 3 | Search Ontology: | |
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Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS7 gene on chromosome 19p13.3. (2) | ||
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Ontology: | Human Disease ( DOID:0112093 ) |
OTHER nuclear type mitochondrial complex I deficiency 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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