Search Ontology:
Human Disease
nuclear type mitochondrial complex I deficiency
- Term ID
- DOID:0112065
- Synonyms
-
- MC1DN
- Definition
- A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome. (2)
- References
- Ontology
- Human Disease ( DOID:0112065 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models