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