OBO ID: DOID:0111491
Term Name: combined oxidative phosphorylation deficiency 15 Search Ontology:
Synonyms:
  • COXPD15
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation] in MTFMT on chromosome 15q22.31. https://www.ncbi.nlm.nih.gov/pubmed/21907147
References:
Ontology: Human Disease   (DOID:0111491)
OTHER combined oxidative phosphorylation deficiency 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MTFMT Combined oxidative phosphorylation deficiency 15 614947
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None