Term Name:	mitochondrial complex IV deficiency nuclear type 15
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.
Ontology:	Human Disease [DOID:0070500]   ( DOID:0070500 )