Search Ontology:
Human Disease

combined oxidative phosphorylation deficiency 15

Term ID
DOID:0111491
Synonyms
  • COXPD15
Definition
A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation] in the MTFMT gene on chromosome 15q22.31. https://www.ncbi.nlm.nih.gov/pubmed/21907147
References
Ontology
Human Disease   ( DOID:0111491 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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