| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An increased concentration of an amino acid in the urine, due to a decreased kidney functionality . (Human Phenotype Ontology, HP_0008335) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008335 |
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1 genes associated with the renal aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SUCLG1 | succinate-CoA ligase, alpha subunit |