OBO ID: DOID:0112086
Term Name: nuclear type mitochondrial complex I deficiency 26 Search Ontology:
Synonyms:
  • MC1DN26
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFA9 on chromosome 12p13.32. https://pubmed.ncbi.nlm.nih.gov/22114105/
References:
Ontology: Human Disease   (DOID:0112086)
OTHER nuclear type mitochondrial complex I deficiency 26 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFA9 Mitochondrial complex I deficiency, nuclear type 26 618247
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None