Search Ontology:
Human Disease

mitochondrial complex IV deficiency nuclear type 11

Term ID
DOID:0070497
Synonyms
  • MC4DN11
Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX20 gene on chromosome 1q44. (2)
References
Ontology
Human Disease   ( DOID:0070497 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models