OBO ID: DOID:0112089
Term Name: nuclear type mitochondrial complex I deficiency 11 Search Ontology:
Synonyms:
  • MC1DN11
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFAF1 on chromosome 15q15.1. https://pubmed.ncbi.nlm.nih.gov/17557076/
References:
Ontology: Human Disease   (DOID:0112089)
OTHER nuclear type mitochondrial complex I deficiency 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFAF1 Mitochondrial complex I deficiency, nuclear type 11 618234
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None