Search Ontology:
Human Disease

mitochondrial complex IV deficiency nuclear type 15

Term ID
DOID:0070500
Synonyms
  • MC4DN15
Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX8A gene on chromosome 11q13.1. https://pubmed.ncbi.nlm.nih.gov/26685157/
References
Ontology
Human Disease   ( DOID:0070500 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models