OBO ID: DOID:0112075
Term Name: nuclear type mitochondrial complex I deficiency 10 Search Ontology:
Synonyms:
  • MC1DN10
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFAF2 on chromosome 5q12.1. https://pubmed.ncbi.nlm.nih.gov/16200211/
References:
Ontology: Human Disease   (DOID:0112075)
OTHER nuclear type mitochondrial complex I deficiency 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFAF2 Mitochondrial complex I deficiency, nuclear type 10 618233
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None