Search Ontology:
Human Disease

mitochondrial complex IV deficiency nuclear type 10

Term ID
DOID:0070496
Synonyms
  • MC4DN10
Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX14 gene on chromosome 12q13.12. https://pubmed.ncbi.nlm.nih.gov/22243966/
References
Ontology
Human Disease   ( DOID:0070496 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models