Parent term(s)
Term with siblings
COX deficiency, benign infantile mitochondrial myopathy +
French Canadian Leigh disease
Leigh disease
mitochondrial complex IV deficiency nuclear type 23
COX deficiency, infantile mitochondrial myopathy +
COX deficiency, benign infantile mitochondrial myopathy +
French Canadian Leigh disease
Leigh disease
mitochondrial complex IV deficiency nuclear type 23
denotes an 'is-a' relationship