Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 12
- Term ID
- DOID:0112099
- Synonyms
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- MC1DN12
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24. https://pubmed.ncbi.nlm.nih.gov/17262856/
- References
- Ontology
- Human Disease ( DOID:0112099 )
- is a type of
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