OBO ID: DOID:0112067
Term Name: nuclear type mitochondrial complex I deficiency 25 Search Ontology:
Synonyms:
  • MC1DN25
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous and compound heterozygous mutation in NDUFB3 on chromosome 2q33.1. https://pubmed.ncbi.nlm.nih.gov/22277967/
References:
Ontology: Human Disease   (DOID:0112067)
OTHER nuclear type mitochondrial complex I deficiency 25 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFB3 Mitochondrial complex I deficiency, nuclear type 25 618246
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None