Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 30
- Term ID
- DOID:0112098
- Synonyms
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- MC1DN30
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFB11 gene on chromosome Xp11.3. https://pubmed.ncbi.nlm.nih.gov/26741492/
- References
- Ontology
- Human Disease ( DOID:0112098 )
- is a type of
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