OBO ID: DOID:0112085
Term Name: nuclear type mitochondrial complex I deficiency 19 Search Ontology:
Synonyms:
  • MC1DN19
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in FOXRED1 on chromosome 11q24.2. https://pubmed.ncbi.nlm.nih.gov/20818383/
References:
Ontology: Human Disease   (DOID:0112085)
OTHER nuclear type mitochondrial complex I deficiency 19 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FOXRED1 Mitochondrial complex I deficiency, nuclear type 19 618241
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None