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ENGenetic Recurrent Myoglobinuria
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Genetic Recurrent Myoglobinuria is related to cox deficiency, benign infantile mitochondrial myopathy and mitochondrial myopathy. An important gene associated with Genetic Recurrent Myoglobinuria is LPIN1 (Lipin 1), and among its related pathways/superpathways are TP53 Regulates Metabolic Genes and Cytoprotection by HMOX1. Affiliated tissues include skeletal muscle and kidney, and related phenotypes are recurrent myoglobinuria and muscle weakness
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MALACARDS
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MGI
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