Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 25
- Term ID
- DOID:0112067
- Synonyms
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- MC1DN25
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous and compound heterozygous mutation in the NDUFB3 gene on chromosome 2q33.1. https://pubmed.ncbi.nlm.nih.gov/22277967/
- References
- Ontology
- Human Disease ( DOID:0112067 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models