Search Ontology:
Human Disease

nuclear type mitochondrial complex I deficiency 27

Term ID
DOID:0112090
Synonyms
  • MC1DN27
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MTFMT gene on chromosome 15q22.31. https://pubmed.ncbi.nlm.nih.gov/22499348/
References
Ontology
Human Disease   ( DOID:0112090 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models