Term Name: COX deficiency, benign infantile mitochondrial myopathy
Synonyms: Isolated cytochrome C oxidase deficiency
Definition: A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.
Ontology: Human Disease [DOID:0081377]   ( DOID:0081377 )

Relationships
is a type of: cytochrome-c oxidase deficiency disease
has subtype: mitochondrial complex IV deficiency nuclear type 1 mitochondrial complex IV deficiency nuclear type 3 mitochondrial complex IV deficiency nuclear type 4 mitochondrial complex IV deficiency nuclear type 7 mitochondrial complex IV deficiency nuclear type 8 mitochondrial complex IV deficiency nuclear type 10 mitochondrial complex IV deficiency nuclear type 11 mitochondrial complex IV deficiency nuclear type 12 mitochondrial complex IV deficiency nuclear type 14 mitochondrial complex IV deficiency nuclear type 15 mitochondrial complex IV deficiency nuclear type 16 mitochondrial complex IV deficiency nuclear type 17 mitochondrial complex IV deficiency nuclear type 18 mitochondrial complex IV deficiency nuclear type 19 mitochondrial complex IV deficiency nuclear type 20 mitochondrial complex IV deficiency nuclear type 21 mitochondrial complex IV deficiency nuclear type 22