| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003652 |
| Similar Terms | |
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1 genes associated with the recurrent myoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| COQ2 | coenzyme Q2 4-hydroxybenzoate polyprenyltransferase |
