OBO ID: DOID:0112065
Term Name: nuclear type mitochondrial complex I deficiency Search Ontology:
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 nuclear type mitochondrial complex I deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None