Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 24
- Term ID
- DOID:0112079
- Synonyms
-
- MC1DN24
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB9 gene on chromosome 8q24.13. https://pubmed.ncbi.nlm.nih.gov/22200994/
- References
- Ontology
- Human Disease ( DOID:0112079 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models