Myoglobinuria, Recurrent (RM-MT)

Myoglobinuria, Recurrent, also known as recurrent myoglobinuria mitochondrial, is related to acquired idiopathic sideroblastic anemia and cox deficiency, benign infantile mitochondrial myopathy. An important gene associated with Myoglobinuria, Recurrent is MT-CO1 (Mitochondrially Encoded Cytochrome C Oxidase I), and among its related pathways/superpathways are Metabolism and Thermogenesis. Affiliated tissues include skeletal muscle, and related phenotypes are ragged-red muscle fibers and exercise-induced myoglobinuria