Search Ontology:
Human Disease
mitochondrial type mitochondrial complex I deficiency
- Term ID
- DOID:0112100
- Synonyms
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- MC1DM
- Definition
- A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the mitochondrial genome. https://pubmed.ncbi.nlm.nih.gov/22972949/
- References
- Ontology
- Human Disease ( DOID:0112100 )
- is a type of
-
- has subtype
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