Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency 8
- Term ID
- DOID:0112081
- Synonyms
-
- MC1DN8
- Definition
- A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS3 gene on chromosome 11p11.2. https://pubmed.ncbi.nlm.nih.gov/14729820/
- References
- Ontology
- Human Disease ( DOID:0112081 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations