|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Recurring episodes of myoglobinuria, i.e., of the presence of myoglobin in the urine. This is usually a consequence of rhabdomyolysis, i.e., of the destruction of muscle tissue. (Human Phenotype Ontology, HP_0003652)|
|Downloads & Tools|
1 genes associated with the recurrent myoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|COQ2||coenzyme Q2 4-hydroxybenzoate polyprenyltransferase|