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 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models