Term Name:	mitochondrial complex IV deficiency nuclear type 10
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.
Ontology:	Human Disease [DOID:0070496]   ( DOID:0070496 )