Term Name:	mitochondrial complex IV deficiency nuclear type 22
Synonyms:	MC4DN22
Definition:	A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX16 gene on chromosome 14q24.2.
Ontology:	Human Disease [DOID:0070507]   ( DOID:0070507 )