|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An increased concentration of an amino acid in the urine, due to a decreased kidney functionality . (Human Phenotype Ontology, HP_0008335)|
|Downloads & Tools|
1 genes associated with the renal aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SUCLG1||succinate-CoA ligase, alpha subunit|