OBO ID: DOID:0112073
Term Name: nuclear type mitochondrial complex I deficiency 9 Search Ontology:
Synonyms:
  • MC1DN9
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFS6 on chromosome 5p15.33. https://pubmed.ncbi.nlm.nih.gov/15372108/
References:
Ontology: Human Disease   (DOID:0112073)
OTHER nuclear type mitochondrial complex I deficiency 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFS6 Mitochondrial complex I deficiency, nuclear type 9 618232
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None