OBO ID: DOID:0112094
Term Name: nuclear type mitochondrial complex I deficiency 14 Search Ontology:
Synonyms:
  • MC1DN14
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFA11 on chromosome 19p13.3. https://pubmed.ncbi.nlm.nih.gov/18306244/
References:
Ontology: Human Disease   (DOID:0112094)
OTHER nuclear type mitochondrial complex I deficiency 14 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFA11 Mitochondrial complex I deficiency, nuclear type 14 618236
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None