Term Name:	mitochondrial complex IV deficiency nuclear type 11
Synonyms:	MC4DN11
Definition:	A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX20 gene on chromosome 1q44.
Ontology:	Human Disease [DOID:0070497]   ( DOID:0070497 )