Search Ontology:
Human Disease

mitochondrial complex IV deficiency nuclear type 7

Term ID
DOID:0070494
Synonyms
  • MC4DN7
Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX6B1 gene on chromosome 19q13.12. (2)
References
Ontology
Human Disease   ( DOID:0070494 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models