Search Ontology:
Human Disease

combined oxidative phosphorylation deficiency 26

Term ID
DOID:0111490
Synonyms
  • COXPD26
Definition
A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the TRMT5 gene on chromosome 14q23.1. https://www.ncbi.nlm.nih.gov/pubmed/26189817
References
Ontology
Human Disease   ( DOID:0111490 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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