Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 11
- Term ID
- DOID:0112089
- Synonyms
-
- MC1DN11
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF1 gene on chromosome 15q15.1. https://pubmed.ncbi.nlm.nih.gov/17557076/
- References
- Ontology
- Human Disease ( DOID:0112089 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models